Main
|
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
|
ClinicalTrials.gov |
Last refreshed on:
|
12 December 2020 |
Main ID: |
NCT03425162 |
Date of registration:
|
01/02/2018 |
Prospective Registration:
|
Yes |
Primary sponsor: |
|
Public title:
|
Ultrasound Guided Anterior Quadratus Lumborum Block
|
Scientific title:
|
Ultrasound Guided Anterior Quadratus Lumborum Block for Postoperative Pain After Percutaneous Nephrolithotomy: Randomized Controlled Trial |
Date of first enrolment:
|
February 12, 2018 |
Target sample size:
|
60 |
Recruitment status: |
Completed |
URL:
|
https://clinicaltrials.gov/show/NCT03425162 |
Study type:
|
Interventional |
Study design:
|
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Outcomes Assessor).
|
Phase:
|
N/A
|
|
Countries of recruitment
|
Turkey
| | | | | | | |
Contacts
|
Name:
|
Korgün Ökmen, M.D |
Address:
|
|
Telephone:
|
|
Email:
|
|
Affiliation:
|
University of Health Sciences, Bursa Yuksek Ihtisas Training and Research Hospital |
| | |
Key inclusion & exclusion criteria
|
Inclusion Criteria:
- Patients who were in the American Society of Anesthesiologists (ASA) I-III class and
underwent elective Percutaneous nephrolithotomy
Exclusion Criteria:
- Previous history of opioid use preoperatively,
- Allergy to local anesthetics,
- The presence of any systemic infection,
Age minimum:
20 Years
Age maximum:
60 Years
Gender:
All
|
Health Condition(s) or Problem(s) studied
|
Ultrasound
|
Postoperative Pain
|
Intervention(s)
|
Procedure: Group P
|
Drug: Morphine Sulfate
|
Procedure: Group A
|
Primary Outcome(s)
|
Visual Analog Scale
[Time Frame: Postoperative 24 hours]
|
Secondary Outcome(s)
|
side effect profile
[Time Frame: Postoperative 24 hours]
|
morphine consumption
[Time Frame: Postoperative 24 hours]
|
additional analgesic use
[Time Frame: Postoperative 24 hours]
|
Source(s) of Monetary Support
|
Please refer to primary and secondary sponsors
|
Results
|
Results available:
|
|
Date Posted:
|
|
Date Completed:
|
|
URL:
|
|
|
|