Trials / Unknown
UnknownNCT02767544
Vaginal Wound Infiltration Analgesia for Postoperative Pain After Laparoscopic Hysterectomy: a Randomized Trial
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 81 (actual)
- Sponsor
- Helsinki University Central Hospital · Academic / Other
- Sex
- —
- Age
- 30 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
In cases of laparoscopic hysterectomy , women were randomized to two groups: ropivacaine ( vaginal wound infiltration analgesia) vs. control group. Results regarding postoperative pain and need of oxycodone.
Detailed description
Women assigned to laparoscopic hysterectomy were randomly divided into two groups as regard surgery: a ropivacaine group (RG) (n=41) and a control group (CG) (n=40). General anesthesia and use of local anesthetics were standardized. Visual analog scale (VAS) scores for pain and side effects (nausea/vomiting) and the amount of postoperative analgesic used were recorded for 24 hours.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Vaginal wound local analgesia after laparoscopic hysterectomy |
Timeline
- Start date
- 2014-11-01
- Primary completion
- 2016-10-01
- Completion
- 2016-10-01
- First posted
- 2016-05-10
- Last updated
- 2016-05-10
Source: ClinicalTrials.gov record NCT02767544. Inclusion in this directory is not an endorsement.