Skip to content

Determination of the Minimum Effective Concentration of Ropivacaine for Rectus Sheath Combined with Transversus Abdominis Plane Block in Elderly Patients with Different Muscle Mass Undergoing Laparoscopic Radical Resection of Colorectal Cancer: A Prospective, Double-Blind Clinical Study

Determination of the Minimum Effective Concentration of Ropivacaine for Rectus Sheath Combined with Transversus Abdominis Plane Block in Elderly Patients with Different Muscle Mass Undergoing Laparoscopic Radical Resection of Colorectal Cancer: A Prospective, Double-Blind Clinical Study - Determination of the Minimum Effective Concentration of Ropivacaine for Rectus Sheath Combined with Transversus Abdominis Plane Block in Elderly Patients with Different Muscle Mass Undergoing Laparoscopic Radical Resection of Colorectal Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115567
Enrollment
Unknown
Registered
2025-12-29
Start date
2025-12-29
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

Low Muscle Mass Group:Nerve block with different concentrations of ropivacaine
Normal Muscle Mass Group:Nerve block with different concentrations of ropivacaine

Sponsors

First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.The patient has a full understanding of the study, voluntarily participates in it, and signs the informed consent form. 2.Patients who are scheduled to undergo laparoscopic colon or rectal cancer surgery. 3.American Society of Anesthesiologists (ASA) physical status classification is Grade ?–?. 4.Aged 65 years or above, regardless of gender.

Exclusion criteria

Exclusion criteria: 1.Patients with neuromuscular diseases, cognitive dysfunction, allergies to anesthetic drugs, a history of opioid abuse, coagulation disorders, or liver and kidney failure. 2.Infection or damage near the puncture site. 3.Cases where the patient refuses to sign the informed consent form to participate in the study. 4.Other circumstances that the researchers deem inappropriate for participation in this trial.

Design outcomes

Primary

MeasureTime frame
Whether the block is successful or not,Minimum Effective Concentration of Ropivacaine;

Secondary

MeasureTime frame
The NRS scores of patients at rest and during movement were measured at 3, 6, 12, and 24 hours postoperatively.;Intraoperative opioid consumption;Total postoperative opioid consumption;Number of effective presses of the postoperative analgesic pump;Incidence of adverse reactions such as postoperative nausea, vomiting and dizziness;Plasma ropivacaine concentration;Time to first ambulation;Patient satisfaction score;

Countries

China

Contacts

Public ContactLiZhiwen

First Hospital of Jilin University

lizhiwen@jlu.edu.cn+86 188 4317 7788

Outcome results

None listed

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