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Trial · NCT03380533

Buprenorphine Transdermal Patches in Arthroscopic Rotator Cuff Repair

NCT03380533, Phase 2, Phase 3, Completed, Hospital Italiano de Buenos Aires

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Buprenorphine Transdermal Patches in Arthroscopic Rotator Cuff Repair. Trials, record NCT03380533. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03380533

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Buprenorphine Transdermal Patches in Arthroscopic Rotator Cuff Repair
NCT number
NCT03380533
Status
Completed
Phases
Phase 2, Phase 3
Enrollment
50 participants, actual
Lead sponsor
Hospital Italiano de Buenos Aires
Conditions
Rotator Cuff Tear, Rotator Cuff Injury, Analgesics, Opioid, Buprenorphine
Interventions
Buprenorphine, Placebo Patch, Multimodal Oral Scheme, Tramadol, Placebo Tablet
First posted
2017-12-21
Last updated
2021-04-08

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPain perceptionFive dayssubjective perception of pain through the use of an analogous visual scale
SecondaryConsumption of rescue opiodsFive Daysconsumption of rescue opiods
SecondaryHours of sleep5 dayshours of sleep
SecondaryPerception of Sickness5 dayspresence or not of nausea
SecondaryReadmissions rate5 daysrecord of hospital readmissions for pain or complications related to the use of buprenorphine patches
SecondaryMisuse or abuse of opioids rateFourth month post operatoryBehaviors of misuse or abuse of opioids after the immediate postoperative period

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03380533

GET https://conductscience.org/api/trials/v1/NCT03380533/registered