Effect of epidural anesthesia on the quality of short-term rehabilitation in hospital after surgery for cancer

A retrospective study on the postoperative short-term rehabilitation quality of patients with cancer undergoing minimally invasive radical resection based on thoracic epidural anesthesia (TEA) combined with general anesthesia in comparison with general anesthesia alone

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ISRCTN

Registry ID

ISRCTN16446449

Enrollment

100

Registered

2021-10-26

Start date

2018-01-01

Completion date

Unknown

Last updated

2021-11-08

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

Conditions

Effect of intraoperative thoracic epidural anesthesia on the quality of hospital short-term rehabilitation after minimally invasive radical resection of cancer Surgery

Interventions

Patients undergoing minimally invasive surgery with cancer under general anesthesia according to whether TEA was used in anesthesia, the patients were divided into two groups, namely the TEA group and

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients aged 18 - 80 years undergoing minimally invasive surgery with cancer under general anesthesia

Exclusion criteria

Exclusion criteria: 1. Patients with abnormal blood coagulation indices through the laboratory examination 48 h before operation 2. Patients with the operation time exceeding 12 h 3. Patients with operative method changed to thoracotomy or laparotomy 4. Patients with exploratory thoracotomy or laparotomy within 48 h after the operation

Design outcomes

Primary

Measure	Time frame
Measured using patient records: 1. Dosage of anesthesia and vasoactive drugs used throughout the procedure 2. Postoperative analgesic information, including the time of the first pressing (i.e., the time when the surgery is over), the consumption of analgesic drugs, and the resting and motorial analgesic scores (R-VAS and M-VAS) at 24, 48 and 72 h postoperatively	—

Secondary

Measure	Time frame
Measured using patient records: 1. Demographic information: sex, age, height and weight, smoking and drinking history, preoperative complication of cardiovascular disease, diabetes mellitus, before the operation 2. Duration of the operation (min)	—

Countries

China

Contacts

Public ContactZhaoju Li

wftuyx02@163.com+86 15602405803

Outcome results

None listed

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