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Trial · NCT05609682

Effect of Gabapentin on Post-Operative Pain in Minimally Invasive Sacrocolpopexy

NCT05609682, Early phase 1, Completed, University of Oklahoma

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Effect of Gabapentin on Post-Operative Pain in Minimally Invasive Sacrocolpopexy. Trials, record NCT05609682. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05609682

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Trial

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

Title
Effect of Gabapentin on Post-Operative Pain in Minimally Invasive Sacrocolpopexy
NCT number
NCT05609682
Status
Completed
Phases
Early phase 1
Enrollment
40 participants, actual
Lead sponsor
University of Oklahoma
Conditions
Post Operative Pain
Interventions
Gabapentin, Placebo
First posted
2022-11-08
Last updated
2024-12-06

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryExamine the efficacy of gabapentin in changing postoperative pain scores2 weeks post-opMeasured using the validated surgical pain scale in which 0 (minimum value) means no pain sensation and 10 (maximum value) means most intense pain imaginable
SecondaryPost-operative opioid consumption2 weeks post-opPatients will be asked the number remaining opiate medications left at their follow up visit.
SecondaryPatient satisfaction2 weeks post-op
Patient satisfaction will be obtained using the Pelvic Floor Disability Index questionnaire in which the symptom scale ranges from 0 = not present to 4 = quite a bit in relation to symptoms and how much they bother the participant.
SecondaryDegree of somnolence2 weeks post-opThe Pelvic Floor Impact Questionnaire measures how symptoms affect activities, relationships and feelings, ranging from Not at all to Quite a bit.

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.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT05609682

GET https://conductscience.org/api/trials/v1/NCT05609682/registered