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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03805269
Other study ID # SNUBHTAP
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date March 14, 2019
Est. completion date December 31, 2024

Study information

Verified date January 2024
Source Seoul National University Bundang Hospital
Contact Bon-Wook Koo, Dr.
Phone +82-10-7227-1379
Email tendong2@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There have been some studies to compared trans abdominis plane(TAP) block with wound infiltration of local anesthetics in multiport laparoscopic surgery, but there have been no studies in single incision laparoscopic gastrectomy. The purpose of this study was to compare the effect of ultrasonography-guided transverse nerve block and localized anesthesia infiltration in patients with single incision laparoscopic gastrectomy.


Description:

Patients were randomly divided into group N(ultrasonography-guided TAP) block and group W( before surgery local anesthetic infiltration at the incision site). We compared the opioid usage, postoperative 6, 24, and 48 hours pain, presence of vomiting, and duration of hospitalization during the operation.


Recruitment information / eligibility

Status Recruiting
Enrollment 94
Est. completion date December 31, 2024
Est. primary completion date December 28, 2024
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - ASA class I-II - Age: >18 Exclusion Criteria: - patients of severe kidney & liver dysfunction - allergy of local anesthetics

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
TAP block
TAP block: local anesthetics infiltration at trans abdominis plane
wound infiltration
wound infiltration: local anesthetics infiltration at surgical incision

Locations

Country Name City State
Korea, Republic of Seoul National Universuty, Bundang Hospital Seongnam-si Gyonggido

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary post operative pain score 100 mm scale of visual analogue scale 4 hours after end of surgery
Secondary post operative opioid consumption total amount of opioid 4 hours after end of surgery
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