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Effect of Postoperative Analgesia with Tapentadol Fumarate on the Quality of Recovery in Patients Undergoing Laparoscopic Radical Resection for Colorectal Cancer

Effect of Postoperative Analgesia with Tapentadol Fumarate on the Quality of Recovery in Patients Undergoing Laparoscopic Radical Resection for Colorectal Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115404
Enrollment
Unknown
Registered
2025-12-25
Start date
2025-12-31
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Colorectal cancer

Interventions

Tegileridine Fumarate group (T group):Tiglitazidine for postoperative analgesia
Sufentanil group (S group):Sufentanil for postoperative analgesia

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Age 18–64 years; 2. Scheduled for elective laparoscopic radical surgery for colorectal cancer; 3. American Society of Anesthesiologists (ASA) physical status I–III; 4. Normal preoperative cognitive function (MoCA score >=26), no history of anxiety or depression, no long-term use of sedative-hypnotics or opioids.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of allergies to related drugs or contraindications; 2. Patients with severe neurological diseases (such as epilepsy, post-stroke sequelae), psychiatric disorders (such as schizophrenia), or cognitive impairments before surgery; 3. Patients with severe cardiopulmonary or liver and kidney dysfunction; 4. Patients who have undergone radiotherapy, chemotherapy, or immunotherapy before surgery, as well as those with other malignant tumors; 5. Patients unable to cooperate with scale assessments after surgery; 6. Patients requiring transfer to the intensive care unit (ICU) for further treatment after surgery.

Design outcomes

Primary

MeasureTime frame
QoR-15 score;

Secondary

MeasureTime frame
MoCA score;Time of first postoperative gas passage, defecation, and eating;Adverse reactions within 72 hours after surgery;time to first rescue analgesia; patient satisfaction ;VAS pain score at rest and during movement;

Countries

China

Contacts

Public ContactSheng Wang

The First Affiliated Hospital of University of Science and Technology of China

iamsheng2020@ustc.edu.cn+86 191 5600 7726

Outcome results

None listed

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