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Clinical Trials/CTRI/2020/04/024740
CTRI/2020/04/024740
Not yet recruiting
Phase 2

A randomized single blind comparative clinical study of Bala Taila and Tila Taila yoni pichu and matra basti in sukhprasava

ational Institute of Ayurveda0 sites0 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: O629- Abnormality of forces of labor, unspecified
Sponsor
ational Institute of Ayurveda
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Patient willing and able to participate in study with written informed consent.
  • 2\.Pregnant women of age between 20\-40 years.
  • 3\.Gestational age after 35 weeks.
  • 4\.Pregnant women of height 150\-170cm.
  • 5\.Pregnant women of weight 45\-75kg.
  • 6\.Hemoglobin more than 10 gm%

Exclusion Criteria

  • 1\.Primigravidae over 35 years of age.
  • 2\.Grand multiparae i.e. parity \>4\.
  • 3\.History of previous LSCS along with Bad obstetric history.
  • 4\.Pregnancy associated with Pregnancy induced hypertension, Pre\-eclampsia, Eclampsia, Gestational Diabetes, Placenta previa, Abruptio placentae.
  • 5\.Patients with Cephalo\-pelvic disproportion.
  • 6\.Patients with any systemic disorder like Diabetes Mellitus, Renal disorder, Cardiac disorder, Tuberculosis, Bronchial asthma.
  • 7\.Patients with pathology of Reproductive system like Uterine or Cervical fibroid, Benign or Malignant tumor , Fothergill repair, Recto vaginal fistula, Vesico vaginal fistula, Ovarian cyst.
  • 8\.Past history of complication during previous pregnancy or labor like Abruptio placentae,
  • Postpartum haemorrhage, Intra uterine fetal death.

Outcomes

Primary Outcomes

Not specified

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