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Clinical Trials/CTRI/2021/03/032275
CTRI/2021/03/032275
Not yet recruiting
Phase 4

To study efficay of sublingual Misoprostol vs intravenous Tranexamic acid in reducing amount of blood loss in full term pregnant women undergoing primary LSCS :A randomized control trial

Aarupadi Veedu Medical College and Hoppital0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: O94-O9A- Other obstetric conditions, not elsewhere classified
Sponsor
Aarupadi Veedu Medical College and Hoppital
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

Sponsor
Aarupadi Veedu Medical College and Hoppital

Eligibility Criteria

Inclusion Criteria

  • Full term women undergoing primary Cesarean Section at Aarupadi Veedu Medical College and Hospital who are willing to participate

Exclusion Criteria

  • 1\)Previous Cesarean Section
  • 2\)Induced/augmented labour
  • 4\)chorioamnionitis
  • 5\)antepartum hemorrhage
  • 6\)pre term pregnancy
  • 7\)overdistension\-multipregnancy,polyhydromnios

Outcomes

Primary Outcomes

Not specified

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