Skip to content

Effect of transvaginal natural orifice transluminal endoscopic surgery on mode of delivery: a prospective study

Effect of transvaginal natural orifice transluminal endoscopic surgery on mode of delivery: a prospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100042404
Enrollment
Unknown
Registered
2021-01-21
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Diseases of obstetrics and gynecology

Interventions

No history of transvaginal posterior fornix laparoscopic surgery:Nil
There was a history of transvaginal posterior fornix laparoscopic surgery:Nil

Sponsors

Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Subjects aged 18-40 years old; 2. Full term pregnant subjects with a history of transvaginal posterior fornix endoscopic surgery; 3. The subjects with certain education level have better reading comprehension ability; 4. Subjects of American Society of anesthesiologists (a) grade 1-11; 5. Patients who understand the protocol and are willing to participate in the study should provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with medical complications (such as hypertension, diabetes, heart disease, kidney disease, etc.); 2. Patients with pregnancy complications (such as gestational diabetes mellitus, gestational hypertension, intrahepatic cholestasis of pregnancy, etc.) 3. Subjects with twin pregnancy; 4. Patients with history of uterine surgery; 5. Patients with history of cesarean section; 6. Subjects with abnormal fetal position; 7. Patients with pelvic outlet stenosis; 8. Macrosomia; 9. Subjects with fetal distress; 10. Umbilical cord around neck >= 3 times; 11. Body temperature > 37.5 degrees C; HB < 80g / L; 12. Subjects with a history of transumbilical single port laparoscopic surgery; 13. Subjects who participated in other clinical trials within three months before participating in this experiment; 14. Subjects with mental illness or drug abuse that may affect compliance with the requirements of this trial.

Design outcomes

Primary

MeasureTime frame
Natural birth rate;Conversion rate of cesarean section;

Secondary

MeasureTime frame
Cesarean section rate;Vaginal fornix laceration rate;total stage of labor;

Countries

China

Contacts

Public ContactYujian Jia

Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China

236640366@qq.com+86 13094429439

Outcome results

None listed

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