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

Analysis of the feasibility and safety of day surgery for total hysterectomy 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
ChiCTR2100042255
Enrollment
Unknown
Registered
2021-01-17
Start date
2021-01-18
Completion date
Unknown
Last updated
2021-04-19

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

Conditions

Gynecological diseases

Interventions

case series:ERAS+LESS+Day surgery

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
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Aged 45-65 years; 2) Patients who need total hysterectomy due to gynecological diseases; 3) American Society of Anesthesiologists (A) Grade 1-11; 4) Patients willing to choose day surgery; 5) Patients can understand this Plan and willing to participate in the study, provide written informed consent.

Exclusion criteria

Exclusion criteria: 1) Body temperature > 37.4 degrees C; 2) Hb < 80g/L; 3) Highly suspected malignant; 4) With internal and surgical complications such as hypertension, diabetes, heart disease, etc., which have not been effectively controlled; 5) With acute reproductive tract Inflammation; 6) Have a history of multiple abdominal surgery, severe pelvic adhesions; 7) Participated in other clinical trials within three months before participating in this experiment; 8) There is already a mental illness or drug abuse that may affect compliance with the requirements of this experiment Circumstances; 9) Circumstances deemed unsuitable by other researchers to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
operation time;Intraoperative blood loss;Perioperative complications;Whether to transfer to porous laparoscopy or open surgery;whether to transfer to the general ward;Whether to return to surgery unplanned;First exhausted 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;Patient's life quality scale;Rehospitalization rate 30 days after surgery;Patient satisfaction;

Secondary

MeasureTime frame
Hospital costs;

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