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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03241875
Other study ID # Nakhli anesthesia sahloul
Secondary ID
Status Completed
Phase Phase 4
First received July 29, 2017
Last updated September 28, 2017
Start date December 1, 2016
Est. completion date September 28, 2017

Study information

Verified date September 2017
Source Faculty of Medicine, Sousse
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the effect of premedication with pregabalin or gabapentin versus placebo on postoperative shoulder pain after laparoscopic cholecystectomy.


Description:

Preoperative premedication with gabapentins reduces preoperative anxiety, stress response to surgical stimuli, decreases anesthetic use. The incidence of postoperative nausea and vomiting appears to be decreased. The other desired effect of gabapentins is the reduction in the intensity of postoperative pain after laparoscopic surgery.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date September 28, 2017
Est. primary completion date August 30, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- uncomplicated laparoscopic cholecystectomy

- American Society of Anesthesiologists (ASA) status < 3

Exclusion Criteria:

- acute cholecystitis

- conversion to open cholecystectomy

- history of epilepsia, psychiatric disorders and cognitive impairment

- Pregnancy and breastfeeding

- allergy to pregabalin and/or gabapentin

- Chronic pain

- Chronic medication by corticosteroids, neuroleptics or non steroidal anti inflammatory drugs

Study Design


Intervention

Drug:
Pregabalin 75mg
In this group, premedication is performed with 2 capsules of pregabalin 2 hours before anesthetic induction.
Gabapentin 300mg
In this group, premedication is performed with 2 capsules of gabapentin 2 hours before anesthetic induction.
Placebo oral capsule
In this group, no premedication is performed, but patients receive 2 capsules of placebo 2 hours before anesthetic induction.

Locations

Country Name City State
Tunisia Sahloul Teaching Hospital Sousse

Sponsors (1)

Lead Sponsor Collaborator
Faculty of Medicine, Sousse

Country where clinical trial is conducted

Tunisia, 

References & Publications (3)

Agarwal A, Gautam S, Gupta D, Agarwal S, Singh PK, Singh U. Evaluation of a single preoperative dose of pregabalin for attenuation of postoperative pain after laparoscopic cholecystectomy. Br J Anaesth. 2008 Nov;101(5):700-4. doi: 10.1093/bja/aen244. Epub — View Citation

Tiippana EM, Hamunen K, Kontinen VK, Kalso E. Do surgical patients benefit from perioperative gabapentin/pregabalin? A systematic review of efficacy and safety. Anesth Analg. 2007 Jun;104(6):1545-56, table of contents. Review. — View Citation

Valadan M, Banifatemi S, Yousefshahi F. Preoperative Gabapentin to Prevent Postoperative Shoulder Pain After Laparoscopic Ovarian Cystectomy: A Randomized Clinical Trial. Anesth Pain Med. 2015 Dec 5;5(6):e31524. doi: 10.5812/aapm.31524. eCollection 2015 D — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Post operative shoulder pain Primary outcome is the intensity of shoulder pain during the first 48 hours after laparoscopic cholecystectomy using the visual analog scale (VAS). VAS score with rest at 2h, 6h, 12h, 24h and 48 hours after surgery
Secondary remifentanil consumption during anesthesia Remifentanil requirements during anesthesia were calculated (µg/kg/mn) one hour after tracheal tube removal
Secondary Post operative sleep quality during the first night Patient's sleep quality was assessed during the first postoperative night by the Spiegel score. first night after surgery
Secondary Post operative nausea and vomiting The intensity of post operative nausea and vomiting was assessed by a 0 to 3 score (0: no nausea or vomiting, 1: slight mild nausea, 2: moderate nausea, 3: vomiting). 2, 6, 12, 24 and 48 hours after surgery.
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