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Ultrasound-guided Transversus Abdominis Plane Block Combined with Ilioinguinal/Iliohypogastric Nerve Block for Analgesia After Laparoscopic gynecological Surgery: A Randomized Double-Blinded Dose-comparison Trail

Ultrasound-guided Transversus Abdominis Plane Block Combined with Ilioinguinal/Iliohypogastric Nerve Block for Analgesia After Laparoscopic gynecological Surgery: A Randomized Double-Blinded Dose-comparison Trail

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005739
Enrollment
Unknown
Registered
2014-12-31
Start date
2015-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

laparoscopic gynecological surgery

Interventions

Group TAP-low:0.25% ropivacaine 15ml for TAP block, saline 15ml for IIN block
Group TAP+IIN:0.25% ropivacaine 15ml for TAP block, 0.25% ropivacaine 15ml for IIN block
Group TAP-high:0.5% ropivacaine 15ml for TAP block, saline 15ml for IIN block

Sponsors

Department of Anesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-60 years; 2. ASA status: I to III; 3. gynecological laparoscopic surgery using general anesthsia; 4. the operation time: 2h+/-30min; 5. understand the prupose of the clincal experiment and take signiture.

Exclusion criteria

Exclusion criteria: 1. body mass index (BMI) more than at least 35kg/m2; 2. opioid use or substance abuse; 3. nervous system diseases; 4. participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Numerical Rating Scale with movement at 12h after surgery;

Secondary

MeasureTime frame
Total opioid consumption and additional analgesia request;anesthesiologists' satisfaction with local anesthetic deposition;NRS scores at rest and with movement at 0h, 30min, 1h, 2h, 4h, 6h, 8h, 12h, 24h;presence and severity of PONV and Sedation at 0h, 30min, 1h, 2h, 4h, 6h, 8h, 12h, 24h;Total antiemetic and antipruritic consumption at 0h, 30min, 1h, 2h, 4h, 6h, 8h, 12h, 24h;

Countries

China

Contacts

Public ContactZhang Yi
zy83743670@sina.com+86 13986039131

Outcome results

None listed

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