A Randomised control trial to look at antibiotic prophylaxis in operative vaginal delivery.
Not Applicable
- Conditions
- Health Condition 1: O860- Infection of obstetric surgical woundHealth Condition 2: O861- Other infection of genital tract following deliveryHealth Condition 3: O85- Puerperal sepsisHealth Condition 4: O864- Pyrexia of unknown origin following deliveryHealth Condition 5: O862- Urinary tract infection followingdelivery
- Registration Number
- CTRI/2022/08/044547
- Lead Sponsor
- Christian Medical College and Hospital Vellore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Women aged 16 years or above, willing and able to give informed consent.
2.Women who have had an operative vaginal delivery at 36+0 completed weeks or greater gestation.
Exclusion Criteria
1.Clinical indication for continuation of antibiotic administration post-delivery
2.Known allergy to penicillin or to any of the components of co-amoxiclav, as previously identified
3.History of anaphylaxis to another �²-lactam agent (e.g. cephalosporin, carbapenem or monobactam)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method