Outcome of modified Misgav Ladach (MML) method in first and second time caesarean deliveries

Outcome of modified Misgav Ladach (MML) method in first and second time caesarean deliveries: a non-randomised controlled single-centre trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN26532492

Enrollment

200

Registered

2009-02-19

Start date

2008-11-15

Completion date

Unknown

Last updated

2015-01-13

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

Conditions

Caesarean deliveries Pregnancy and Childbirth

Interventions

This trial is taking place at the Istanbul Bakirkoy Maternity and Children's Hospital, Department of Obstetrics and Gynaecology. Approximately 200 patients will be recruited, 50 patients in each of

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. Term pregnancies >36 weeks of gestation 2. No age limit

Exclusion criteria

Exclusion criteria: 1. Intrauterine infection 2. Anaemia (37.5 Celsius) 6. Use of antibiotics in the last 7 days 7. Placenta previa 8. Abruptio placenta 9. Severe preeclampsi and Hellp syndrome

Design outcomes

Primary

Measure	Time frame
Surgical outcomes: 1. Operation time 2. Time until delivery of neonate 3. APGAR score 4. Haemoglobin 5. Haematocrit 6. Surgical complications	—

Secondary

Measure	Time frame
Post-operative outcomes: 1. Hospital stay 2. Febrile morbidity 3. Scar complications 4. Infection 5. Post-operative recovery Secondary outcomes 2 to 5 were assessed 2 and 7 days after caesarean operation. However, patients who experienced any problem were followed-up until resolution of the problem.	—

Countries

Turkey

Outcome results

None listed

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