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Efficacy of Transversus Abdominis Plane Block for Acute Postoperative Pain Relief in Kidney Recipients, a Double Blinded Clinical Trial

Efficacy of Transversus Abdominis Plane Block for Acute Postoperative Pain Relief in Kidney Recipients, a Double Blinded Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201012185264N3
Enrollment
44
Registered
2012-09-20
Start date
2010-11-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

kidney recipiet,s patients. kidney transplant status

Interventions

Intervention 1: In study group:22 patients were blocked by 15 ml bupivacaine 0.5% + 5 micro-gram/ml epinephrine on the side of surgery and ultrasound guide after induction of anesthesia.The probe w
Treatment - Drugs
Placebo
In study group:22 patients were blocked by 15 ml bupivacaine 0.5% + 5 micro-gram/ml epinephrine on the side of surgery and ultrasound guide after induction of anesthesia.The probe was inserted betw
In control group ,20 ml normal saline was injected in transverse abdominis neurofascial plane under sonography guide after induction of anesthesia at the side of surgery.The probe was inserted betwee

Sponsors

Vice Chancellor for research,Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1) ASA class II and III patients 2) Aged 15–65 year who were scheduled as kidney recipients under general anesthesia Exclusion criteria: 1)Addiction to opioids 2) Long term usage of antidepressants, antipsychotics, anticonvulsants, clonidine 3) Patients with coagulopathy and hepatomegaly.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Postoperative pain. Timepoint: at 1st , 4th , 8th , 12th and 24h following surgery. Method of measurement: numeric rating scale.

Secondary

MeasureTime frame
Intraoperative and first 24 hours opioids consumption. Timepoint: At the end of operation and end of first 24 hours after operation. Method of measurement: Dose calculation in mg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSussan Soltani Mohammadi

Tehran university of medical sciences

soltanmo@sina.tums.ac.ir+98 21 2229 5296

Outcome results

None listed

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