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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03751540
Other study ID # Blocks in LC
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2018
Est. completion date November 26, 2018

Study information

Verified date November 2018
Source Maltepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

the investigators use usually a plane block for postoperative analgesia; if it suitable. İn laparoscopic patients; investigators used oblique subcostal transversus abdominis plane block; formerly. But in the last few months, the investigators have performed serratus intercostal (BRILMA) block with bilateral rectus sheath block. in this retrospective evaluation, the aim of the retrospective evaluation is to determine the effects of two block on postoperative opioid consumption.


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date November 26, 2018
Est. primary completion date November 1, 2018
Accepts healthy volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- patients undergoed laparoscopic cholecystectomy ASA I-II-III

Exclusion Criteria:

- patients used another block or block combination

- no block performed patients

- procedure converted to open procedure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ostap
this block is performed under general anesthesia in this patients for postoperative analgesia.
SIPB plus rectus sheath block
this block is performed under general anesthesia in this patients for postoperative analgesia.

Locations

Country Name City State
Turkey Maltepe University faculty of medicine Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Maltepe University

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Chen Y, Shi K, Xia Y, Zhang X, Papadimos TJ, Xu X, Wang Q. Sensory Assessment and Regression Rate of Bilateral Oblique Subcostal Transversus Abdominis Plane Block in Volunteers. Reg Anesth Pain Med. 2018 Feb;43(2):174-179. doi: 10.1097/AAP.0000000000000715. — View Citation

Fernández Martín MT, López Álvarez S, Pérez Herrero MA. Serratus-intercostal interfascial block as an opioid-saving strategy in supra-umbilical open surgery. Rev Esp Anestesiol Reanim. 2018 Oct;65(8):456-460. doi: 10.1016/j.redar.2018.03.007. Epub 2018 May 20. English, Spanish. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary opioid consumption Tramadol consumption in Patient Controlled Analgesia device and additional and rescue analgesic using 24 hours
Secondary Pain assessed by NRS Changes in Numeric Rating Scale (NRS) at rest and on movement will be recorded at intervals. NRS is a unidimensional measure of pain intensity in adults. The NRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable"). 24 hours
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