-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-276-ocd-appendix-h.xlsx
January 01, 2023 - ES 95% CI SE P-Value Favors Strength
25721185 Torp 2015 GPA NordLOTS, stage 1 14 weeks (post-treatment … 0.35 -1.79 to 2.49 0.75 NS Neutral (Nonsignificant)
25721185 Torp 2015 GPA NordLOTS, stage 1 14 weeks … 7-11 Strength unclear (Continuous predictors; P<0.05)
25721185 Torp 2015 GPA NordLOTS, stage 1 14 weeks … 0.15 -0.45 to 0.74 0.631 NS Neutral (Nonsignificant)
25721185 Torp 2015 GPA NordLOTS, stage 1 14 weeks … B 0.06 -0.01 to 0.13 0.83 NS Neutral (Nonsignificant)
25721185 Torp 2015 GPA NordLOTS, stage 1 14 weeks
-
effectivehealthcare.ahrq.gov/sites/default/files/arthritis-horizon-scan-high-impact-1506.pdf
June 01, 2015 - , and 4 weeks, followed by one
subcutaneous (SC) injection (75 mg) every 4 weeks;3 or secukinumab was … and 4 weeks, followed by one SC injection (75 or 150 mg) every 4
weeks. … , followed by one SC injection every
4 weeks. … ,36 or as three loading doses by IV infusion 10 mg/kg, at baseline, 2 weeks, and 4
weeks, followed … , and 4 weeks,
followed by one SC injection (75 or 150 mg) every 4 weeks.
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-250-cannabis-tables-e1-e4-2022-update_0.xlsx
January 01, 2022 - mg per 100 mcl oromucosal spray (Sativex) titrated to max 6 doses with stable dosing for further 3 weeks … , crossover to ibuprofen 400 mg/day for 8 weeks 0.5 mg/day Ibuprofen 400 mg/day for 8 weeks, crossover … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cannabis-2022-update-surv-rep-1-app-F1-4.xlsx
January 01, 2022 - mg per 100 mcl oromucosal spray (Sativex) titrated to max 6 doses with stable dosing for further 3 weeks … , crossover to ibuprofen 400 mg/day for 8 weeks 0.5 mg/day Ibuprofen 400 mg/day for 8 weeks, crossover … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-250-cannabis-2025-surv-rep-update-table-e5.xlsx
January 01, 2025 - , Median) Pain Duration, Months Psychiatric Comorbidity % N Interventions Dose Treatment Duration (Weeks … duration for use of Strainprint app (tracking app used to obtain data on medicinal cannabis use): 31 weeks … NA
CBD: 202.18 (SD 345.23) 12 weeks (3 months) Short A vs. … of CBD mg/day: 20.00 (20.00 to 40.00)
Median (IQR) dosage of THC mg/day: 25.00 (10.00 to 115.00) 52 weeks … B
Modified pain disability index, weeks 2 to 24 (95% CI −67.78 to -64.01 vs. −45.23 to −41.46), p<0.001
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/Appendix-E-Evidence-Tables-E1-E4_0.xlsx
May 29, 2025 - mg per 100 mcl oromucosal spray (Sativex) titrated to max 6 doses with stable dosing for further 3 weeks … , crossover to ibuprofen 400 mg/day for 8 weeks 0.5 mg/day Ibuprofen 400 mg/day for 8 weeks, crossover … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone … , cross over to ibuprofen 400 mg/day for 8 weeks Ibuprofen 400 mg/day for 8 weeks, crossover to nabilone
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/main-apps-surv-report-2-acute-pain.pdf
May 01, 2022 - ; 2
weeks to less than 4 weeks; 4 weeks or longer? … ; 2 weeks to
less than 4 weeks; 4 weeks or longer? … ; 2 weeks to less than 4 weeks; 4 weeks or longer? … ; 2
weeks to less than 4 weeks; 4 weeks or longer? … ; 2 weeks to 4 weeks;
≥4 weeks
NOTE: There will not be exclusion criteria for
duration, unless duration
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/ocr-protocol-final_1.pdf
December 18, 2019 - low-risk nulliparous
pregnant women (the ARRIVE trial)5 demonstrated that induction of labor at 39 weeks … , 39 to
41 weeks, >41 weeks)
• Pregnant women ≥37
weeks undergoing CR
in the outpatient
setting … , 39 to 41
weeks, >41 weeks)
• Pregnant women ≥37
weeks undergoing CR
in the outpatient
setting … , 39 to 41
weeks, >41 weeks)
• Pregnant women ≥37
weeks undergoing CR
with a prostaglandin … , 39 to
41 weeks, >41 weeks)
Women with
contraindications to CR
in the outpatient setting:
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-250-cannabis-surveillance-report-3_0.pdf
May 01, 2022 - reviewed evidence, in patients with chronic (mainly
neuropathic) pain with short-term treatment (4 weeks … Key Question 2: Harms of cannabinoids for chronic pain compared with placebo in the
short term (4 weeks … 8 to 12 weeks 4 to 47 weeks 4 and 12 weeks 4 weeks
Abbreviations: CBD = cannabidiol; CBDV = cannabidivarin … Eligible observational studies must have assessed a mean duration of
treatment of at least 4 weeks, … Withdrawal due to adverse events for comparable THC to CBD ratio versus placebo (short-term, 4 weeks
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-250-cannabis-apps-a-e-surveillance-report-2-final_0_0.pdf
March 01, 2022 - Overall, in patients with chronic (mainly neuropathic) pain with short-term treatment (4
weeks to < … Key Question 2: Harms of cannabinoids for chronic pain compared with placebo in the
short term (4 weeks … The
findings are applicable to short-term treatment (4 weeks to <6 months) in patients with chronic … 8 to 12 weeks 4 to 47 weeks 4 and 12 weeks 4 weeks
Abbreviations: CBD = cannabidiol; CBDV = cannabidivarin … Eligible observational studies must have assessed a mean duration of
treatment of at least 4 weeks,
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/arthritis-psoriatric_surveillance.pdf
March 01, 2013 - A new meta-analysis9 found PsA
Response Criteria (PsARC)
response at 12-14 weeks was
significantly … ACR20 response at
12-16 weeks was greater for both
anti-TNFs and other biologics. … ACR70 response at 12-16 weeks
was greater with both anti-TNFs
and other biologics than with
placebo … for at least 28 weeks.
78.2% had at least one adverse
event (AE), but only 4.6% had a
No safety … PsA Response Criteria
(PsARC) response at
12-14 weeks was
greater for anti-TNFs
than placebo (
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-250-cannabis-2024-surv-rep-update-executive-sum.pdf
January 01, 2024 - In
patients with chronic (mainly neuropathic) pain with short-term treatment (4 weeks to
<6 months) … We included RCTs and comparative observational studies
with a minimum of 4 weeks duration that assessed … 5.3 to 7.3) 6.75 (4.00 to 8.67)e 6.01 (4.67 to 7.4)f 6.28 (6.12 to 6.44)
Study Duration 4 to 15 weeks … 4 to 47 weeks 4 to 16 weeks 4 weeks
Abbreviations: CBD = cannabidiol; CBDV = cannabidivarin; MS = … Key Question 2: Harms of cannabinoids for chronic pain compared with placebo in the
short term (4 weeks
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cannabis-2023-surv-rep-4-table-E-5.xlsx
January 01, 2023 - , Median) Pain Duration, Months Psychiatric Comorbidity % N Interventions Dose Treatment Duration (Weeks … NA
CBD: 202.18 (SD 345.23) 12 weeks (3 months) Short A vs. … to -50.1 vs. -24.9 to -22.2)
LS mean difference: −27.84 (95% CI −29.71 to −25.96), p<0.001
PIX from weeks … B
Modified pain disability index, weeks 2 to 24 (95% CI −67.78 to -64.01 vs. −45.23 to −41.46), p<0.001 … B
MFHW, weeks 2 to 24: (95% CI 46.24 to 50.46 vs. 5.75 to 1.53), p<0.001
MFHW- mental component summary
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cannabis-2022-surv-rep-4-table-F5.xlsx
January 01, 2022 - , Median) Pain Duration, Months Psychiatric Comorbidity % N Interventions Dose Treatment Duration (Weeks … NA
CBD: 202.18 (SD 345.23) 12 weeks (3 months) Short A vs. … to -50.1 vs. -24.9 to -22.2)
LS mean difference: −27.84 (95% CI −29.71 to −25.96), p<0.001
PIX from weeks … B
Modified pain disability index, weeks 2 to 24 (95% CI −67.78 to -64.01 vs. −45.23 to −41.46), p<0.001 … B
MFHW, weeks 2 to 24: (95% CI 46.24 to 50.46 vs. 5.75 to 1.53), p<0.001
MFHW- mental component summary
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-265-radiation-bone-disease-disposition-comments.pdf
August 29, 2023 - pain is assessed (for example in one study data
was included that was only at 2 weeks post treatment … For meta-analyses looking at
post-RT up to 4 weeks, if studies
reported earlier time frames, we
used … the data closest to the
4 weeks for pooled data
represented in figure 3 comparing
SF and MF EBRT. … Upon review of our data in the
meta-analysis, 2 studies reported
data for less than 4 weeks:
Foro … Arnalot 2008 at 3 weeks and
the RR was 0.87 (95% CI 0.75 to
1.02).
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/type-2-diabetes-medications-update_surveillance.pdf
December 31, 2013 - weeks 0.001). … and to 11.1+/- 9.9% after 12 weeks. … Change in
HbA1c
Cross-over: 52 weeks of sitagliptin changed HbA1c by −0.9% from
baseline, but … Significant weight reductions occurred after switching to liraglutide for 26
weeks: from 92.8 ± 20.6 … Canagliflozin 100 and
300 mg provided reductions from baseline in body weight over 26 weeks,
placebo
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-250-cannabis-2025-surv-rep-update-executive-sum.pdf
January 01, 2025 - ratio) products.4-6 In patients with chronic (mainly neuropathic)
pain with short-term treatment (4 weeks … 6.4 to 7.30) 6.75 (4.00 to 8.67)e 6.01 (4.67 to 7.40)f 4.77 (2.54 to 6.28)
Study Duration 4 to 15 weeks … 4 to 47 weeks 4 to 16 weeks 4 to 12 weeks
Abbreviations: CBD = cannabidiol; CBDV = cannabidivarin … 6.35 (6.1 to 6.6) 4.98 (4.58 to
5.31)
4.4 (4.39 to 4.41) 4.32 (4.31 to 4.33)
Study Duration,
Weeks … Key Question 2: Harms of cannabinoids for chronic pain compared with placebo in the
short term (4 weeks
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/gerd-2005_executive.pdf
January 01, 2005 - (between classes and within class)
PPIs were superior to H2RAs in resolution of
GERD symptoms at 4 weeks … and healing of
esophagitis at 8 weeks. … difference between omeprazole,
lansoprazole, pantoprazole, and rabeprazole for
relief of symptoms at 8 weeks … difference in the comparison of esomeprazole
20 mg with omeprazole 20 mg in relief of
symptoms at 4 weeks … omeprazole 20 mg, there was
a significant difference in favor of esomeprazole
for relief of symptoms at 4 weeks
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-250-cannabis-2024-surv-rep-update-table-e5.xlsx
January 01, 2024 - , Median) Pain Duration, Months Psychiatric Comorbidity % N Interventions Dose Treatment Duration (Weeks … NA
CBD: 202.18 (SD 345.23) 12 weeks (3 months) Short A vs. … to -50.1 vs. -24.9 to -22.2)
LS mean difference: −27.84 (95% CI −29.71 to −25.96), p<0.001
PIX from weeks … B
Modified pain disability index, weeks 2 to 24 (95% CI −67.78 to -64.01 vs. −45.23 to −41.46), p<0.001 … B
MFHW, weeks 2 to 24: (95% CI 46.24 to 50.46 vs. 5.75 to 1.53), p<0.001
MFHW- mental component summary
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/depression-treatment-ssri_surveillance.pdf
January 01, 2013 - Outcomes did not differ
between the groups at 10
weeks. … Remission rates did
not differ among arms at 8
weeks. … Outcomes did not differ from
those of placebo group at 4
weeks. … Treatment
assignment did not predict
outcomes (remission or time
to remission) at 48 and 72
weeks … to
55 weeks
Overall
response rate
for all active
tx was 52%.