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Effect of transumbilical laparo-endoscopic Single-Site Surgery on mode of delivery: a prospective study

Effect of transumbilical laparo-endoscopic Single-Site Surgery on mode of delivery: a prospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100042376
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 gynecolog

Interventions

with the history of transumbilical laparo-endoscopic single-site surgery:Nil
no history of transumbilical laparo-endoscopic single-site 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) Aged between 18-40 years; 2) Full term pregnancies with a history of transumbilical laparo-endoscopic single-site surgery; 3) Have a certain degree of education and good reading comprehension ability; 4) American Society of anesthesiologists (a) grade I-II; 5) Patients can understand the protocol and are willing to participate in the study, and 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) Twin pregnancy; 4) History of uterine surgery; 5) History of cesarean section; 6) Abnormal fetal position; 7) The pelvic outlet was narrow; 8) Macrosomia; 9) Fetal distress; 10) Umbilical cord around the neck for more than 3 times; 11) Body temperature > 37.5 degrees C, Hb < 80g / L; 12) with a history of transvaginal posterior fornix laparo-endoscopic surgery; 13) Participated in other clinical trials within three months before participating in this experiment; 14) There are already cases of mental illness or drug abuse that may affect compliance with the test requirements.

Design outcomes

Primary

MeasureTime frame
Natural birth rate;Incidence of umbilical incisional hernia;

Secondary

MeasureTime frame
Cesarean section rate;Conversion rate of cesarean section;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