Ultrasound Guided Subcostal Transversus Abdominis Plane Versus Paravertebral Block in the Laparoscopic Cholecystectomy
NCT02379780 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2015-03-06
Summary
The investigators aimed to compare the effects of perioperative anesthesia consumption of ultrasound guided subcostal transversus abdominis plane and paravertebral block in laparoscopic cholecystectomy.
Conditions
- Cholecystitis
Interventions
- PROCEDURE
-
USG guided Subcostal TAP block
Ultrasonography Assisted Subcostal TAP blockage: In plane technique was applied and 22 G needle (BRAUN Stimuplex D Plus 0,71\*50 mm 22G\*2) was used. Intravascular injection was eliminated after the passage of rectus sheath by negative aspiration. 0,5-1 ml local anesthetic was applied directly to confirm the right place. 10 cc bupivacain ( 0,5 % Marcain flacon, Astra Zeneca, Sweeden) and 5 cc lidocaine was injected to the site. The same procedure was applied to the opposite site. we investigated amount of TIVA during the operation, postoperative Visual Analog Scores and the time that the pain free time.
- PROCEDURE
-
USG guided Paravertebral Block
Ultrasonoraphy assisted Thoracic Paravertebral blockage application: In-plane or out-of-plane technique was used with stimuplex needle (BRAUN Stimuplec D Plus 0,71\*50 mm 22 G\* 2'', 15°). Popping sensation that was felt by the penetration of the internal intercostal membrane, guided to paravertebral space. Intravascular injection was eliminated by negative aspiration. 0,5 - 1 ml local anesthetic injection was administered to show the displacement of pleura downward that confirmed the place of the needle in the right place. Then 10 cc bupivacain (% 0.5 Marcaine® flacon, Astra Zeneca, Sweeden) and 5 cc lidocaine was injected to the site. we investigated amount of TIVA during the operation, postoperative Visual Analog Scores and the time that the pain free time.
Sponsors & Collaborators
-
Erzincan University
collaborator OTHER -
Cukurova University
lead OTHER
Principal Investigators
-
ILKE KUPELI · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
-
ZEHRA BEDİR · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
-
HUSEYIN EKEN · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
-
UFUK KUYRUKLUYILDIZ · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
-
DIDEM ONK · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
-
ORHAN BINICI · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
-
AYSIN ALAGOL · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
-
GULDANE KARABAKAN · MENGUCEK GAZI TRAINING AND RESEARCH HOSPİTAL
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-09-30
- Primary Completion
- 2015-01-31
- Completion
- 2015-02-28
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