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NCT06176573
Pre-operative Versus Post-operative Vaginal Cleansing With Chlorhexidine Solution in Prevention Post-Cesarean Section Infection
NA trial testing Chlorhexidine in Post Cesarean Infectious Morbidity in 120 participants. Completed in 31 August 2021.
31 August 2021
Quick facts
| Lead sponsor | Federal Teaching Hospital Abakaliki |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | prevention |
| Enrollment | 120 |
| Start date | 1 April 2021 |
| Primary completion | 31 August 2021 |
| Estimated completion | 31 August 2021 |
| Sites | 1 location across Nigeria |
Drugs / interventions tested
- Chlorhexidine (CHLORHEXIDINE) — full drug profile →
Conditions studied
- Post Cesarean Infectious Morbidity — all drugs for Post Cesarean Infectious Morbidity →
Sponsor
Federal Teaching Hospital Abakaliki
Who can join
Adults 18 to 44, female only, with Post Cesarean Infectious Morbidity. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Maternal infectious morbidity is a common complication of cesarean delivery, especially in a poor recourse setting like ours. This study was done to compare the effectiveness of preoperative vaginal cleansing with immediate postoperative vaginal cleansing with chlorhexidine solution in preventing post-cesarean infectious morbidities. Randomized trial involving 120 consented women who had elective or emergency cesarean sections at term, 60 in each group. Group 1 had preoperative while group 2 had postoperative vaginal cleansing with 1% chlorhexidine.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06176573
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Related trials
Other trials of Chlorhexidine
Trials testing the same drug.
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- NCT07058727 — Different Hemostatic Agents Used in Partial Pulpotomy on Pulp Survival and Postoperative Pain · NA · recruiting
- NCT06627270 — Antibiotic Treatment Effects on Intratumoral Bacteria Modulation in Surgical Patients With Oral Cancer · Phase 2 · recruiting
- NCT07197073 — Antibacterial Effect of Ozonated Olive Oil, Propolis and Chlorhexidine Mouthwashes in Pediatric Patients · NA · completed
- NCT06667089 — Povidone-Iodine Versus Chlorhexidine in Surgical Wound Care · NA · completed
Other Federal Teaching Hospital Abakaliki trials
Trials by the same sponsor.
- NCT06960850 — Effects of Oral Propranolol on Induction-Delivery Interval During Induction of Labour With Oxytocin · NA · not yet recruiting
- NCT07474350 — Valethamate Bromide Versus Hyoscine Butyl Bromide in Reducing Labour Duration Among Primigravida · NA · completed
- NCT06126068 — Comparison of Loading Dose Magnesium Sulphate With Prichard Regimen in the Management of Severe Preeclampsia and Eclamps · NA · completed
- NCT07394491 — Intravenous Paracetamol Versus Intramuscular Tramadol in Shortening the Duration of Labour. · NA · completed
- NCT06220279 — Efficacy of Single Dose Rectal Diclofenac With Oral Diclofenac for the Relief of Perineal Pain Within 24 Hours After Epi · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06176573 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Federal Teaching Hospital Abakaliki
- Last refreshed: 19 December 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06176573.
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