# Baylor Research Institute: Observational study in Surgical Site Infection, Vaginal Cuff Cellulitis (900 participants)

**Score:** 55/100

| Field | Value |
|---|---|
| Sponsor | Baylor Research Institute |
| Sponsor type | Academic and hospital |
| Study | Prevention of Vaginal Cuff Infection After Hysterectomy by Addition of Vaginal Clindamycin |
| NCT ID | NCT07888101 |
| Phase | Observational |
| Status | enrolling by invitation |
| Conditions | Surgical Site Infection; Vaginal Cuff Cellulitis; Bacterial Vaginosis |
| Intervention types | drug |
| Target enrollment | 900 |
| Site countries | United States |
| Posted | 2026-10-22 |
| Planned start | 2026-12 |
| Event | Newly registered study |
| Event date | 2026-10-22 |

## Why this score
- Posted in the last two weeks.
- 900 participants planned.

Source: ClinicalTrials.gov (U.S. National Library of Medicine) API v2 (https://clinicaltrials.gov/study/NCT07888101). Last refreshed: 2026-11-04T06:04:38.232Z.
From public ClinicalTrials.gov registrations. Sponsor and study level only: we never list investigators, contacts or participants. A registration describes a planned study and can change. Status changes are read from each study's current status, actual dates and latest posted update, not a full change history, so an update can be a correction rather than a new change. Verify on ClinicalTrials.gov.