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Analgesic effect of peripheral nerve block after gynecological lower abdominal surgery; concentration versus volume of local anesthetic.A prospective randomized trial.

Analgesic effect of peripheral nerve block after gynecological lower abdominal surgery; concentration versus volume of local anesthetic.A prospective randomized trial. - Analgesic effect of peripheral nerve block after gynecological lower abdominal surgery; concentration versus volume of local anesthetic.A prospective randomized trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019766
Enrollment
48
Registered
2015-11-12
Start date
2013-10-29
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients who are scheduled for gynecological lower abdominal surgery.

Interventions

Patinets will receive ultrasound-guided transversus abdominis plane block using 0.4%,3 mg/kg of ropivacaine. Patinets will receive ultrasound-guided transversus abdominis plane block using 0.2%,3 mg/k

Sponsors

Nagoya University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1)Patients who are scheduled for gynecological lower abdominal surgery in Nagoya university hospital. 2)American Society of Anethesiologists physical status in 1, 2 or 3. 3)Patients who can evaluate the pain using visual analogue scale(VAS) 4)Patients who can give written informed consent,

Exclusion criteria

Exclusion criteria: 1)Patients who have stomach ulcer, renal failure or liver failure. 2)Patients who have allergy to the drugs which will going to use in this trial. 3)Patients who have severe obesity over BMI 30. 4)Patients who have contraindication of Ropivacaine. 5)Patients who are regarded ineligible by doctors with ather reasons.

Design outcomes

Primary

MeasureTime frame
Postoperative morphine consumption after 4, 24, 48, and 72 hours.Using patient controlled analgesia.

Secondary

MeasureTime frame
Pain:Visual analogue scale(VAS) at rest and at cough after 4, 24, 48, and 72 hours postoperation. Adverse event. Blood pressure and SpOs after 4,24,48 and 72 hours postoperation, Ropivacaine plasma concentration after 0,15,30,45,60 and 120 mins after transversus abdominis plane block.

Countries

Japan

Contacts

Public ContactAkiko Akane

Nagoya University Hospital Department of Anethesiology

a-ohashi@med.nagoya-u.ac.jp052-744-2340

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026