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Transcutaneous electrical acupoint stimulation improves postoperative sleep in patients with gastrointestinal tumors by regulating Nrf2/ARE signaling pathway

Transcutaneous electrical acupoint stimulation improves postoperative sleep in patients with gastrointestinal tumors by regulating Nrf2/ARE signaling pathway

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054971
Enrollment
Unknown
Registered
2021-12-29
Start date
2021-12-30
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

gastrointestinal tumor

Interventions

Group 1:transcutaneous electrical stimulation
Group 2:fake stimulus

Sponsors

Xuzhou Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with elective laparoscopic gastric and colorectal tumor surgery; 2. Aged 18 to 75 years; 3. American Society of Anesthesiologists (ASA) grades I to III; 4. BMI 18.5-28kg/m^2; 5. Preoperative clinical tumor TNM staging: cTis-3N0-1M0 (refer to AJCC/UICC 8th edition TNM staging).

Exclusion criteria

Exclusion criteria: 1. Pittsburgh sleep quality index scale score> 7 points; 2. Sleep apnea, or moderate snoring; 3. Severe sinus bradycardia (heart rate below 50 beats/min) or sinus node disease, second- or third-degree atrioventricular block, and pacemaker before surgery; 4. Long-term use of anticonvulsants, antidepressants or other psychotropic drugs; 5. Those who are hypersensitive or allergic to the research drugs or equipment; 6. Severe heart, liver or kidney disease; 7. Participated in other clinical trials within the past 3 months; 8. Have hearing and language communication barriers, unable to communicate effectively with doctors; 9. Patients who are pregnant or breastfeeding; 10. Patients with fever or infection before surgery; 11. Patients who live with critically ill patients or live in the same ward with more than 3 people.

Design outcomes

Primary

MeasureTime frame
PSQI score;Athens Insomnia Score;

Secondary

MeasureTime frame
Visual Analogue Scale Score;Heart rate variability (HRV) physiological data;Intraoperative blood pressure;Intraoperative remedies;Operation time;Anesthesia time;Liquid in and out;Body temperature changes;Analgesic use;Adverse events and medication;Time of first air exhaust after operation;Hospital stay;

Countries

China

Contacts

Public ContactLu Feifei

Xuzhou Hospital of Traditional Chinese Medicine

lufei09flg@126.com+86 18795425961

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026