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Effect of total intravenous anesthesia and combined intravenous and inhalation anesthesia on postoperative fatigue of patients undergoing laparoscopic hysterectomy

Effect of total intravenous anesthesia and combined intravenous and inhalation anesthesia on postoperative fatigue of patients undergoing laparoscopic hysterectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033861
Enrollment
Unknown
Registered
2020-06-14
Start date
2020-06-19
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Postoperative fatigue (POF)

Interventions

Intravenous anesthesia group (Group P):Narcotization was conducted under EEG monitoring. TCI propofol (2.5 -- 3.5 g/ mL) and Remifentanil (1.5-2.5ng/ml) was administered to maintain Narcotrend at D0-2
Combined anesthesia group (Group S):Narcotization was conducted under EEG monitoring.Inhalation of 1.5-2.5% sevoflurane, minimum effective alveolar concentration (MAC) was maintained at 0.7, TCI remif

Sponsors

The Second Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 74 Years

Inclusion criteria

Inclusion criteria: 1. Over 45 years old and under 74 years old; 2. American Society of anesthesiologists (ASA) grade: I-II; 3. Patients who have indications for total hysterectomy and decide to perform minimally invasive surgery under laparoscope; 4. Obtain the informed consent of the patient and / or legal guardian, and sign the informed consent;

Exclusion criteria

Exclusion criteria: 1. Patients who received emergency operation within 24 hours after admission; 2. The patients had fatigue symptoms before operation, i.e. visual analogue scale > 5 points; 3. The patient has communication disorder (language disorder, mental disorder) and can't cooperate; 4. If the patient is allergic to a certain drug in the anesthesia program, other drugs should be used instead;

Design outcomes

Primary

MeasureTime frame
Identity-Consequences Fatigue Scale-10, ICFS-10;Visual simulation scale, VAS;

Secondary

MeasureTime frame
Perioperative grip strength examination;Time of first postoperative ambulation;Postoperative anal exhaust time;length of patient stay;

Countries

China

Contacts

Public ContactXue Bai

The Second Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine

378721510@qq.com+86 17820550561

Outcome results

None listed

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