Trials / Completed
CompletedNCT03442218
Use of Antiseptic Solution for Vaginal Wash Before Cesarean Section
Use fo Antiseptic Solution for Vaginal Wash Before Cesarean Section in Patients With Premature Rupture of Membranes. A Randomized, Double Blind, Controlled Trial.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 203 (actual)
- Sponsor
- Saint Thomas Hospital, Panama · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
To evaluate the rate of infections after cesarean sections in patients with premature rupture of membranes after vaginal wash either with an antiseptic solution (clorhexidine solution) vs. saline solution (placebo).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Clorhexidine | Vaginal wash with clorhexidine solution previous to cesarean section in patients with premature rupture of membranes. |
| DRUG | Saline solution | Vaginal wash with saline solution previous to cesarean section in patients with premature rupture of membranes. |
Timeline
- Start date
- 2017-06-01
- Primary completion
- 2017-08-31
- Completion
- 2018-02-28
- First posted
- 2018-02-22
- Last updated
- 2019-12-09
Locations
1 site across 1 country: Panama
Source: ClinicalTrials.gov record NCT03442218. Inclusion in this directory is not an endorsement.