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Clinical Trials/IRCT2015042521917N2
IRCT2015042521917N2
Completed
Phase 2

Comparison of the effects using abdominal binder and routine medical care on clinical outcomes of cesarean section: a randomized controlled trial

Vice chancellor for research, Tabriz University of Medical Sciences0 sites178 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Cesarean.
Sponsor
Vice chancellor for research, Tabriz University of Medical Sciences
Enrollment
178
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Vice chancellor for research, Tabriz University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Inclusion Criteria: First or second parity; elective cesarean section; 18 to 35 years old; having literacy; term pregnancy, singleton and without complicated pregnancy; fannenstiel incision on the skin and Kerr Incision on the uterine; hemoglobin more than 11 g/dl during Pregnancy; no history of substance abuse and smoking; no presence of placenta previa or placenta accreta, Incerta, Percreta at ultrasound; no rupture of membrane more than 6 Hours; permission of gynecologist.
  • Exclusion criteria: Intolerance of abdominal binder by participant; no tendency to continue the study; presence of essential disease based on mother\`s report; increasing the duration of surgery more than one hour; simultaneous surgery such as hysterectomy, myomectomy and tubectomy; preeclampsia or eclampsia; presence of severe bleeding or bleeding leading to hysterectomy; presence of hemorrhagic disorders or use of anticoagulant drugs such as heparin or warfarin; tissues damage during cesarean delivery.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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