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The comparison of the side effects of heparin and enoxaparin in patient with cesarean

A clinical trial to compare the effects of heparin with enoxaparin in patients undergoing cesarean section

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016031427042N1
Enrollment
176
Registered
2016-04-13
Start date
2014-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

caesarean section. Delivery by elective caesarean section

Interventions

Intervention 1: In intervention group Heparin is given 5000 unit, SC twice daily for 7 to 12 days after surgery. Intervention 2: In control group Anoxaparin is prescribed 24 hours following surgery, 4
Treatment - Drugs
In intervention group Heparin is given 5000 unit, SC twice daily for 7 to 12 days after surgery
In control group Anoxaparin is prescribed 24 hours following surgery, 40 mg, SC daily for 7 to 10 days

Sponsors

Vice chancellor for research, Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: The ones who have two of these criteria: age over 35, BMI more than 30, multiparty, preeclampsia, postpartum hemorrhage, emergency cesarean and hysterectomy. Exclusion criteria: patient's discontent, risk of wound infection (diabetes, Chorioamnionitis and long-lasting rupture of the amniotic sac)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Formation of thrombosis in deep veins. Timepoint: During hospital stay period. Method of measurement: Clinical examination and Doppler sonography.;Formation of pulmonary embolus. Timepoint: During hospital stay period. Method of measurement: Clinical examination and CT scan.

Secondary

MeasureTime frame
Formation of hematoma. Timepoint: for 10 days after surgery. Method of measurement: wound examination.;Wound infection. Timepoint: for 10 days after surgery. Method of measurement: wound examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohre Salari

Kerman University of Medical Sciences

zohreh_salari@yahoo.com+98 34 3223 5011

Outcome results

None listed

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