Comparison between the effect of using transamic acid and position on Caesarean section bleeding rate, Surgical team satisfaction and postoperative complications.

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240421061546N1

Enrollment

102

Registered

2024-06-22

Start date

2024-05-28

Completion date

Unknown

Last updated

2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bleeding rate of cesarean section, surgical team satisfaction and postoperative complications..

Interventions

Intervention 1: Intervention group: Group: A is the transzymic acid injection group, in which one gram of transzymic acid will be injected intravenously in cesarean surgery, after the baby is born and

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Term women candidates for cesarean surgery Absence of bleeding coagulation disorders Absence of liver and kidney diseases No history of thromboembolism A history of singletons No history of polyhydramnios, oligohydramnios based on ultrasound Normal CBC (hemoglobin level 15-10 mg/d and platelets <100 thousand)

Exclusion criteria

Exclusion criteria: Dissatisfaction with continuing to participate in the study (during and after surgery) Placental abruption during cesarean section Acreta pair Polyhydramino Oligohydramnios uterine atony Intra-abdominal adhesions Bladder, intestine and other visceral damage during surgery Uterine dilatation Spinal anesthesia during surgery

Design outcomes

Primary

Measure	Time frame
Cesarean section bleeding. Timepoint: Registration of hemoglobin, hematocrit and platelets of the patient before the operation and 6 hours after the operation for all three groups. Method of measurement: Bleeding measurement rate: 1. Based on weighing of gas, lancet and suction volume 2. Satisfaction of the surgical team based on questionnaire 3. Registration of hemoglobin, hematocrit and platelets of the patient before the operation and 6 hours after the operation for all three groups.;Satisfaction of the surgical team. Timepoint: After cesarean section. Method of measurement: Based on the satisfaction questionnaire of the surgical team.	—

Measure

Time frame

Cesarean section bleeding. Timepoint: Registration of hemoglobin, hematocrit and platelets of the patient before the operation and 6 hours after the operation for all three groups. Method of measurement: Bleeding measurement rate: 1. Based on weighing of gas, lancet and suction volume 2. Satisfaction of the surgical team based on questionnaire 3. Registration of hemoglobin, hematocrit and platelets of the patient before the operation and 6 hours after the operation for all three groups.;Satisfaction of the surgical team. Timepoint: After cesarean section. Method of measurement: Based on the satisfaction questionnaire of the surgical team.

—

Secondary

Measure	Time frame
Shoulder pain. Timepoint: In the time period after the surgery in the recovery area of ??the operating room and 24 hours after the surgery. Method of measurement: Visual-linear pain measurement scale (VAS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Dehghan Niri

Mazandaran University of Medical Sciences

elhamdehghanniri@gmail.com+98 35 3725 0742

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026