clinical application of improved uterus incision in placenta previa cesarean section

Randomized controlled clinical trials of improved uterus incision in placenta previa cesarean section in comparison with tradition incision

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-10000983

Enrollment

Unknown

Registered

2010-07-17

Start date

2010-01-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

placenta previa

Interventions

1:traditional Incision

2:improved incision

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of placenta previa,and placenta previa adhere to lower segment of anterior uterine in B ultrasound; 2. Women of childbearing age; 3. without serious liver and kidney dysfunction (ALT, AST, Cr, higher than 1.5 times of upper limit of normal); 4. without serious organic diseases of vital organs (such as heart, liver, kidney) or diabetes TB in previous history; 5. Sign the informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. do not meet the diagnostic criteria of placenta previa; 2. with serious organic diseases of vital organs in previous history; 3. fever; 4. serious infection; 5. with autoimmune disease; 6. other situations that doctors consider should exclude.

Design outcomes

Secondary

Measure	Time frame
The first time getting out of bed after surgery;the first time farting after surgery;volume of blood transfusion;Apgar Score;Incidence of complication;	—

Primary

Measure	Time frame
volume of bleeding in surgery;time of fetus parturition;	—

Countries

China

Contacts

Public ContactZou Li

medzouli@163.com+86 027 85351639

Outcome results

None listed

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