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Comparison of short-term outcomes of two vertical incision in the abdomen and Millard in pregnant women with a previous two time cesarean surgery.

Comparison of short-term outcomes of two vertical incision in the abdomen and Millard in pregnant women with a previous two time cesarean surgery.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012102211205N1
Enrollment
84
Registered
2013-04-22
Start date
2012-11-05
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

Vertical incision and Millard in Pregnant women.

Interventions

Intervention 1: Abdominal vertical incision in 42 patients. Intervention 2: Millard procedure in 42 patients.
Prevention
Abdominal vertical incision in 42 patients
Millard procedure in 42 patients

Sponsors

Vice chancellor for research,Tabriz University of Medical Scienes
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria:Term pregnancy;. history of cesarean section in term pregnancy for more than 2 times; not having an underlying disease such as diabetes or lupus;. not having severe preeclampsia;.no prolonged rupture of membranes (PROM)>= 12 hours, having no oprative bleeding;. Morbid obesity. Exclusion craitria:Midwifery bleeding during surgery ;. including the atonic uterus and placenta acreta ;. placenta percreta ;. need to hysterectomy or ovariectomy ;. need for further explorationduring surgery an underlying disease leading tofutherbleeding ;. such as coagulative disease .Emergency case of midwifery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding. Timepoint: At the end of the abdominal incision. Method of measurement: Using the site of action of counting gases.

Secondary

MeasureTime frame
Time to move the patient lying down, sitting or walking. Timepoint: Every day until discharge. Method of measurement: Tolerable and intolerable pain and need medication and onset of breastfeeding to infants.;Pain scor. Timepoint: Every 4 hours after surgery until discharge. Method of measurement: Using visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Zahra Fardiazar

Tabriz University of Medical Sciences

fardiazar@tbzmed.ac.ir; ro_zavarnia@hotmail.com; wrhrcenter@gmail.com+98 41 1553 9161

Outcome results

None listed

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