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Trial registered on ANZCTR


Registration number
ACTRN12617000260325
Ethics application status
Approved
Date submitted
23/12/2016
Date registered
20/02/2017
Date last updated
20/02/2017
Type of registration
Retrospectively registered

Titles & IDs
Public title
The efficacy of intravenous ibuprofen and pregabalin before laparoscopic cholecystectomy surgery on postoperative pain.
Scientific title
Comparison of pregabalin and pregabalin+ intravenous ibuprofen for preemptive (before the procedure) analgesia for laparoscopic cholecystectomy
Secondary ID [1] 290808 0
Nil known
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
laparoscopic cholecystectomy procedures 301459 0
Condition category
Condition code
Anaesthesiology 301181 301181 0 0
Pain management

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
For postoperative pain we will give one group of patients ( 29 patients for each group) pregabalin 150 mg oral form 1 hour before the operation. The other group will take pregabalin like group 1 and intravenous ibuprofen 800 mg, 1/2 hour before the operation.
Intervention code [1] 296731 0
Treatment: Drugs
Comparator / control treatment
Grup 1 (only pregabalin) is the control group
Control group
Active

Outcomes
Primary outcome [1] 300598 0
postoperative analgesia which evaluated by 100 mm Visual Analog Scale (VAS)
Timepoint [1] 300598 0
postoperative 0,1,2,4,8,12,24, hour
Secondary outcome [1] 330388 0
patient satisfaction score which evaluated by 100 mm visual analog scale.
Timepoint [1] 330388 0
postoperative 1.2.4.8.12.24. hour

Eligibility
Key inclusion criteria
ASA ( american society of anesthesiologists) Physical Status 1-2,
planned for elective laparoscopyc cholecystectomy
Minimum age
18 Years
Maximum age
65 Years
Gender
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Emergency cholecystectomy. Antiepileptic drug use, ASA 3 patient groups, Mild or severe renal insufficiency

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Who is / are masked / blinded?



Intervention assignment
Other design features
Phase
Type of endpoint(s)
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment outside Australia
Country [1] 8527 0
Turkey
State/province [1] 8527 0
Konya

Funding & Sponsors
Funding source category [1] 295232 0
University
Name [1] 295232 0
Baskent University
Address [1] 295232 0
Taskent Caddesi (Eski 1. Cadde) 77. Sokak (Eski 16. Sokak) No:11 06490 Bahcelievler / ANKARA / Turkey
Country [1] 295232 0
Turkey
Primary sponsor type
University
Name
Baskent University
Address
Taskent Caddesi (Eski 1. Cadde) 77. Sokak (Eski 16. Sokak) No:11 06490 Bahcelievler / ANKARA / Turkey
Country
Turkey
Secondary sponsor category [1] 294060 0
None
Name [1] 294060 0
Address [1] 294060 0
Country [1] 294060 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 296574 0
Baskent University Institutional Review Board and Ethics Committee
Ethics committee address [1] 296574 0
Taskent Caddesi (Eski 1. Cadde) 77. Sokak (Eski 16. Sokak) No:11 06490 Bahcelievler / ANKARA / Turkey
Ethics committee country [1] 296574 0
Turkey
Date submitted for ethics approval [1] 296574 0
01/09/2016
Approval date [1] 296574 0
14/10/2016
Ethics approval number [1] 296574 0
KA 16/109

Summary
Brief summary
For managing acute postoperative pain, New medical treatments administered preoperatively. For this purpose, pregabalin has been used previously for laparoscopyc cholecystectomy surgery in some clinical research. Intravenous ibuprofen ( NSAID analgesic) used until 2009. We want to investigate the effect of pregabalin+intravenous ibuprofen used before the operation preemptively on postoperative analgesia for laparoscopyc cholecystectomy.
We enroll 58 patients who undergone elective laparoscopyc cholecystectomy surgery. Exclusion criteria; emergency cholecystectomy, antiepileptic drug use, allergic reaction for study drugs, ASA III-IV patients. mild or severe renal insufficiency.
Group Pregabalin: 1 hour before operation patients will take 150 mg pregabalin oral form.
Group Pregabalin + intravenous ibuprofen: 1 hour before operation patients will take 150 mg pregabalin oral form. Additionally 1/2 hour before operation patients will take 800 mg intravenous ibuprofen.
After operation we give patient controlled analgesia contains fentanyl, and we will evaluate postoperative pain and patient satisfaction.
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 71346 0
Dr Omer Karaca
Address 71346 0
Baskent University Konya Research and Application Center Hocacihan mah saray cad no:1 42080 selcuklu/Konya
Country 71346 0
Turkey
Phone 71346 0
+903322570606
Fax 71346 0
+903322570637
Email 71346 0
dromerkaraca@hotmail.com
Contact person for public queries
Name 71347 0
Dr Omer Karaca
Address 71347 0
Baskent University Konya Research and Application Center Hocacihan mah saray cad no:1 42080 selcuklu/Konya
Country 71347 0
Turkey
Phone 71347 0
+903322570606
Fax 71347 0
Email 71347 0
dromerkaraca@hotmail.com
Contact person for scientific queries
Name 71348 0
Dr Omer Karaca
Address 71348 0
Baskent University Konya Research and Application Center Hocacihan mah saray cad no:1 42080 selcuklu/Konya
Country 71348 0
Turkey
Phone 71348 0
+903322570606
Fax 71348 0
Email 71348 0
dromerkaraca@hotmail.com

No information has been provided regarding IPD availability
Summary results
No Results