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NCT01429480 Clinical Trial

Comparison of TAP (Transversus Abdominis Plane) and Ilioinguinal/Iliohypogastric Nerve Block for Analgesia of Open Inguinal Herniorrhaphy

Pain Clinical Trial

— TAP  

Official title:
Comparison Between Two Ultrasound-guided Blocks (Transversus Abdominis Plane and Ilioinguinal/Iliohypogastric Nerve Blocks) for Pain Relief After Open Inguinal Herniorrhaphy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01429480
Other study ID # 0065-11-HYMC
Secondary ID
Status Recruiting
Phase N/A
First received September 4, 2011
Last updated September 6, 2011
Start date August 2011
Est. completion date August 2013

Study information
Verified date September 2011
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

TAP was recommended by PROSPECT for further investigation as an appropriate analgesic method after open herniorrhaphy. Ilioinguinal/iliohypogastric nerve block is one of the oldest methods of analgesia. The researchers wish to investigate whether the TAP block is as effective as the ilioinguinal/iliohypogastric nerve block?

Recruitment information / eligibility
Status Recruiting
Enrollment 90
Est. completion date August 2013
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients undergoing elective primary unilateral open tension-free mesh inguinal hernia repair

Exclusion Criteria:

- Inability to consent to the study

- BMI more than 40

- Skin infection near injection site

- Chronic hepatic or renal failure

- Peripheral neuropathy

- Proven opioid dependency

- Coagulopathy

- Thrombocytopenia

- Dementia

- Lack of orientation

- Impossibility to understand VAS

- Patients suffering from chronic pain

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Preoperative Ultrasound Guided Ilioinguinal/Iliohypogastric Block

• Preoperative Ultrasound Guided Posterior TAP Block

Drug:
• Patient controlled analgesia

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative pain Intensity of pain in rest and during movement at the operation day and 2 days postoperaive. 2 days postoperatively Yes
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