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Analysis of the feasibility and safety of day surgery for ectopic pregnancy based on enhanced recovery after surgery strategies and single port laparoscopic techniques

Analysis of the feasibility and safety of day surgery for ectopic pregnancy based on enhanced recovery after surgery strategies and single port laparoscopic techniques

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100042371
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

ectopic pregnancy

Interventions

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 45 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18~45 years; 2) Those who are clinically diagnosed as "ectopic pregnancy" require surgical treatment and have stable vital signs; 3) American Society of Anesthesiologists (A) grade I-II; 4) Patients who are willing to choose day surgery; 5) The patient understands the program and is willing to participate in the study, and provides written informed consent.

Exclusion criteria

Exclusion criteria: 1) Body temperature > 37.4 degrees C; 2) Hb < 80g/L; 3) Suspected of massive abdominal hemorrhage and shock manifestations; 4) Those with internal and surgical complications such as hypertension, diabetes, heart disease, etc., which have not been effectively controlled; 5) Acute genital tract inflammation; 6) People with multiple history of abdominal surgery and severe pelvic adhesions; 7) Participated in other clinical trials within three months before participating in this experiment; 8) There has been a mental illness or drug abuse that may affect compliance with the requirements of this test; 9) Other investigators consider it inappropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Whether to return to surgery unplanned;First exhaust time after operation;Time to get out of bed for the first time after surgery;Time of first meal after operation;Visual analoge scale score for postoperative pain;Hospital stay;Whether to delay discharge;Rehospitalization rate 30 days after surgery;Patient satisfaction;Hospital costs;Operation time;Intraoperative blood loss;Perioperative complications;Whether to transfer to porous laparoscopy or open surgery;Whether to transfer to the general ward;

Secondary

MeasureTime frame
Patient's life quality scale;

Countries

China

Contacts

Public ContactXiao-Qin Gan

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

316112248@qq.com+86 13980672233

Outcome results

None listed

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