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Analgesic efficacy of bilateral intertransverse blocks compared with bilateral parasternal blocks in laparoscopic colorectal surgery: a randomized, double-blind, non-inferiority study

Analgesic efficacy of bilateral intertransverse blocks compared with bilateral parasternal blocks in laparoscopic colorectal surgery: a randomized, double-blind, non-inferiority study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068948
Enrollment
Unknown
Registered
2023-03-02
Start date
2023-03-11
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Colorectal tumours

Interventions

Intertransverse block group (ITP group):Patients with bilateral intertransverse block
Thoracic paravertebral block group (TPVB group):Patients with bilateral thoracic paravertebral blocks

Sponsors

Shanghai Jiaotong University Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with colorectal tumor and intended to undergo laparoscopic colorectal surgery; 2. Aged 18-65 years; 3. Sign informed consent; 4. American Society of Anesthesiologists (ASA) grade I-II.

Exclusion criteria

Exclusion criteria: 1. Any relevant major heart or respiratory disease, hematological disease or disorder of coagulation parameters, preexisting major organ dysfunction (e.g., liver or kidney failure); 2. General contraindications of nerve block; 3. Any contraindications for the use of propofol, sufentanil, or sevoflurane; 4. Patients with a history of laparotomy; 5. Patients with previous somatosensory disorders; 6. Patients with spinal anatomic malformations; 7. Patients undergoing emergency surgery; 8. Patients with a long history of opioid use; 9. Patients with mental illness or inability to understand the NRS score.

Design outcomes

Primary

MeasureTime frame
12 hour post-operative motor pain score;

Secondary

MeasureTime frame
Blocking success rate;Numeric rating scale for patient's resting state and cough;Plasma vascular endothelial growth factor-C, IL-6, epinephrine and cortisol levels at 24 hours postoperatively;Degree of nausea and vomiting;Total intra-operative opioid use and total post-operative opioid use;Time to first bowel sounds, time to intestinal exhaust, time to return to activity, and length of hospital stay;Incidence of nerve block-related complications;Quality of patient recovery;

Countries

China

Contacts

Public ContactGu Fei

Shanghai Jiaotong University Affiliated Sixth People's Hospital

xucheng303@163.com+86 151 0213 9984

Outcome results

None listed

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