CTRI/2024/06/069145Not yet recruitingPhase 2
A Randomized comparative clinical trial to evaluate the efficacy of Integrated and Ayurvedic protocol in achieving Sukhaprasava. - NI
ational Institute of Ayurveda Deemed To be University, Jaipur0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Patient with 37th week of gestation with singleton pregnancy and cephalic presentation
- •2. Height 148 to 172cm
- •3. Hemoglobin more than or equal to 10gm%
- •4. Patient with borderline or adequate pelvis
Exclusion Criteria
- •1. History of previous LSCS
- •2. Patient having Bad obstetric history, precious pregnancy
- •3. Pregnancy associated with severe Pregnancy induced hypertension, Pre-eclampsia, Eclampsia, Gestational Diabetes, Placenta previa, Abruptio placentae, severe oligohydramnios, severe polyhydramnios, severe IUGR
- •4. Patients with Cephalo-pelvic disproportion, malpresentation.
- •5. Patients suffering with systemic disorders like Diabetes Mellitus, Renal dysfunction, Cardiac disorder, Tuberculosis, Coagulopathies.
- •6. Patients diagnosed with Benign or Malignant tumor of Reproductive system, Recto vaginal fistula, Vesico-vaginal fistula, second and third degree uterine prolapse
- •7. History of Fothergill repair, Recto vaginal fistula, Vesico-vaginal fistula
- •8. VDRL, HIV, HBsAg positive pregnant woman.
Investigators
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