Trials / Completed
CompletedNCT05192954
Comparing Postoperative Pain After Vessel Sealing Device Versus Conventional Suturing Methods for Vaginal Hysterectomy and Pelvic Reconstructive Surgery
Comparing Postoperative Pain After LigaSureTM Vessel Sealing Device Versus Conventional Suturing Methods for Vaginal Hysterectomy and Pelvic Reconstructive Surgery: a Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 95 (actual)
- Sponsor
- Marlana McDowell · Academic / Other
- Sex
- Female
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
This study will investigate pain outcomes for patients undergoing vaginal hysterectomy with pelvic reconstructive surgery using the LigasureTM vessel sealing device as compared to conventional clamping and suturing methods.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LigaSureTM vessel sealing device | Device will be used to clamp, cauterize, seal, and transect tissue during vaginal hysterectomy. |
Timeline
- Start date
- 2022-01-28
- Primary completion
- 2023-12-30
- Completion
- 2024-10-28
- First posted
- 2022-01-14
- Last updated
- 2024-11-22
Locations
2 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05192954. Inclusion in this directory is not an endorsement.