Cervical incompetence
Conditions
Interventions
1:Transumbilical laparo-endoscopic single-site surgrey for cervical cerclage
2:Porous laparoscopic for cervical cerclage
Sponsors
Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Eligibility
Sex/Gender
Female
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1) Women of childbearing age, aged 20-50 years, with pregnancy plan; 2) According to the diagnosis of cervical incompetence; 3) The vital signs were stable and could tolerate laparoscopic surgery; 4) The patients were able to understand the protocol and were willing to participate in the study. Written consent was provided.
Exclusion criteria
Exclusion criteria: 1) Women without fertility requirements; 2) Women with pregnancy over 14 weeks; 3) Participated in other clinical trials within 3 months before participating in this clinical trial; 4) Patients with severe underlying diseases and unable to tolerate surgical anesthesia; 5) The presence of mental illness or drug abuse that may affect compliance with the trial requirements is known; 6) Human immunodeficiency virus (HIV) infection is known; 7) Other investigators consider it unsuitable for this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Perioperative complications; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual anglogue scale;Body Image Scale/Cosmetic Scale;Pregnancy outcome;Neonatal premature birth rate;Recovery of urination and defecation time after operation;Length of stay;Hospitalization expenses;Patient Satisfaction; | — |
Countries
China
Contacts
Public ContactLi He
Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Outcome results
None listed