Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12616001708448
Ethics application status
Approved
Date submitted
17/11/2016
Date registered
13/12/2016
Date last updated
24/02/2017
Type of registration
Prospectively registered

Titles & IDs
Public title
Postoperative analgesic efficacy of ketamine added to bupivacaine in ultrasound guided transversus abdominis plane block for laparoscopic cholecystectomy
Scientific title
Postoperative analgesic efficacy of ketamine added to bupivacaine in ultrasound guided transversus abdominis plane block for laparoscopic cholecystectomy
Secondary ID [1] 290101 0
nil known
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
postoperative analgesia 301230 0
Condition category
Condition code
Surgery 300076 300076 0 0
Other surgery
Anaesthesiology 300986 300986 0 0
Pain management
Oral and Gastrointestinal 300989 300989 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The patients ' demographic data was recorded. The patients will be divided into two groups. Patients distributed to groups with closed envelope technique
Group I (n=60): control group.
All transversus abdominis plane blocks were performed under ultrasound guidance after induction of anesthesia, before beginning of surgery by the same anesthesiologist who performed block at least 20 times. 1mg/kg Bupivacaine (Marcaine (R) AstraZeneca: Istanbul, Turkey)+ Saline 0.9% (Izotonik sodyum klorur (R) (Eczacibasi: Istanbul, Turkey) ( total 40ml) injected in the transversus abdominis fascial plane under direct visualization.
Group II (n=60): 1mg/kg Bupivacaine (Marcaine (R) AstraZeneca: Istanbul, Turkey)+ 0.5 mg/kg ketamine (Ketalar (R) Pfizer: Istanbul, Turkey)+ Saline 0.9% (Izotonik sodyum klorur (R) (Eczacibasi: Istanbul, Turkey) (total 40ml).

The patients received patient-controlled intravenous analgesia (PCA) with 90 ml normal saline + 500 mg tramadol (Tramosel (R), Haver, Istanbul, Turkey) for postoperative pain management (bolus dose: 5 ml, lockout period: 20 minutes,without loading dose). All patients received intravenous analgesia via the same type of PCA (Patient Controlled Analgesia) device for 24 hours period.
When the pain level is higher than three (0=no pain; 10=severe pain), the patient can use the patient controlled analgesia pump. If the pain still exist, additional analgesic will be applied by the same anesthesiologist who assessed outcomes and the number of additional analgesic was recorded..
Intervention code [1] 295847 0
Treatment: Drugs
Comparator / control treatment
Group II (n=60)
All transversus abdominis plane blocks were performed under ultrasound guidance,
1mg/kg Bupivacaine (Marcaine (R) AstraZeneca: Istanbul, Turkey)+ 0.5 mg/kg Ketamine (Ketalar (R) Pfizer: Istanbul, Turkey)+ Saline 0.9% (Izotonik sodyum klorur (R) (Eczacibasi: Istanbul, Turkey) (total 40ml) injected in the transversus abdominis fascial plane under direct visualization.


Control group
Active

Outcomes
Primary outcome [1] 299547 0
rate of analgesic consumption in the 24 hours after surgery

Datas of analgesic agent consumption are assessed by review of medical records. Analgesic consumption will be calculated by the total amount of analgesic agents spent on Patient-controlled analgesia (PCA)
Timepoint [1] 299547 0
24 hours post surgery
Primary outcome [2] 299548 0
time of first analgesic requirement
this information is taken from patients themselves
Timepoint [2] 299548 0
at any time in the 24 hours
Primary outcome [3] 299549 0
Pain, assessed by visual analogue scale at rest and during movement.
Timepoint [3] 299549 0
at 0-2-4-8-12-24. hours
Secondary outcome [1] 327493 0
Adverse effects (itching, allergies, nausea, vomiting, urinary retention, constipation, respiratory depression, bradycardia, hypotension, dizziness ,hallucination i.e.)
Timepoint [1] 327493 0
during intraoperative process and 24 hours post surgery

Adverse events were recorded. If adverse events were recognized, They were evaluated according to Common Terminology Criteria for Adverse Events (CTC-AE) ver. 4.0.
This adverse events listed are assessed as recorded by treating clinician in the medical records

Eligibility
Key inclusion criteria
elective surgery
laparoscopic cholecystectomy
ASA (American Society of Anesthesiologist) Score) I-II
who can talk turkish language.
Minimum age
18 Years
Maximum age
75 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
blood coagulation pathologies
allergies against local anaesthetics
inability to understand the study protocol
body mass index >30
infection on the block area


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
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Other design features
Phase
Phase 4
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
26/12/2016
Actual
26/12/2016
Date of last participant enrolment
Anticipated
Actual
13/02/2017
Date of last data collection
Anticipated
Actual
14/02/2017
Sample size
Target
120
Accrual to date
Final
108
Recruitment outside Australia
Country [1] 8204 0
Turkey
State/province [1] 8204 0
Bursa

Funding & Sponsors
Funding source category [1] 294472 0
Self funded/Unfunded
Name [1] 294472 0
Demet Ozer
Country [1] 294472 0
Turkey
Funding source category [2] 294634 0
Self funded/Unfunded
Name [2] 294634 0
Derya Karasu
Country [2] 294634 0
Turkey
Primary sponsor type
Individual
Name
Derya Karasu
Address
Bursa Yuksek Ihtisas Training Education Hospital Clinic of Anesthesiology and Reanimation
Mimar Sinan Neighborhood /Emniyet Street/16310 Yildirim/Bursa
Country
Turkey
Secondary sponsor category [1] 293341 0
Individual
Name [1] 293341 0
Canan Yilmaz
Address [1] 293341 0
Bursa Yuksek Ihtisas Training Education Hospital Clinic of Anesthesiology and Reanimation
Mimar Sinan Neighborhood /Emniyet Street/16310 Yildirim/Bursa
Country [1] 293341 0
Turkey

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 295908 0
Yuksek Ihtisas Training and Education Hospital Clinical Researc Ethics Committee
Ethics committee address [1] 295908 0
Ethics committee country [1] 295908 0
Turkey
Date submitted for ethics approval [1] 295908 0
15/08/2016
Approval date [1] 295908 0
05/10/2016
Ethics approval number [1] 295908 0
2011-KAEK-25 2016/17-01

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 68858 0
Dr Demet Ozer
Address 68858 0
Bursa Yuksek Ihtisas Training and Education Hospital Clinic of Anesthesiology and Reanimation Mimar Sinan Neighborhood/ Emniyet Street/ 16310 Yildirim/Bursa
Country 68858 0
Turkey
Phone 68858 0
+9055059045989
Fax 68858 0
Email 68858 0
[email protected]
Contact person for public queries
Name 68859 0
Derya Karasu
Address 68859 0
Bursa Yuksek Ihtisas Training and Education Hospital Clinic of Anesthesiology and Reanimation Mimar Sinan Neighborhood/ Emniyet Street/ 16310 Yildirim/Bursa
Country 68859 0
Turkey
Phone 68859 0
+90505728117
Fax 68859 0
Email 68859 0
[email protected]
Contact person for scientific queries
Name 68860 0
Derya Karasu
Address 68860 0
Bursa Yuksek Ihtisas Training and Education Hospital Clinic of Anesthesiology and Reanimation Mimar Sinan Neighborhood/ Emniyet Street/ 16310 Yildirim/Bursa
Country 68860 0
Turkey
Phone 68860 0
+905057281175
Fax 68860 0
Email 68860 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbasePostoperative analgesic efficacy of ketamine added to bupivacaine in ultrasound guided transversus abdominis plane block for laparoscopic cholecystectomy.2020https://dx.doi.org/10.4328/ACAM.6183
N.B. These documents automatically identified may not have been verified by the study sponsor.