A clinical trail to decrease blood loss after delivery by using suction instrument.
Not Applicable
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2022/11/047649
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All low risk antenatal mothers (nulliparous and multiparous), who are in spontaneous active labour.
Exclusion Criteria
1. Patients posted for Elective LSCS
2. Previous LSCS or previous scarred uterus those are at risk of scar dehiscence.
3. Genital Tract Trauma(Cervical and Vaginal tears) during delivery.
4. Known case of inherited and acquired coagulopathies.
5. Patients with Chorioamnionitis, Prolonged Leaking >24 hours.
6. Patients not willing to give consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of incidence of PPH in control group and study groupTimepoint: within 24 hours after delivery
- Secondary Outcome Measures
Name Time Method 1. Assessment of total blood loss <br/ ><br>2. Uterine tone assessment by measuring symphysio fundal height before application and after removal of suction cannula <br/ ><br>3. Assessment of need for use of any uterotonics, mechanical or surgical methods <br/ ><br>4. Assessment of incidence of infection during postpartum periodTimepoint: within 24 hours after delivery