The Effect Of Tramadol, Metamizol and Dexketoprofen Combination On Chronic Pain Development After Heart Surgery

NCT ID: NCT02660749

Last Updated: 2016-01-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-05-31

Study Completion Date

2016-12-31

Brief Summary

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Non Coronary Heart Surgery scheduled for the study , in patients with acute postoperative period Use of tramadol retard, metamizol and dekxketoprofen the effects on pain and character has been seen in the chronic phase targeted.

Detailed Description

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This prospective study analyzed surgical thoracotomy and sternotomy patients treated with analgesic drug when higher than 4 regularly. Clinical parameters include general demographics, preoperative and postoperative clinical examination status, pain scores, neuropathic pain scores, medication side effects, additional analgesic, antiemetic and lacsatif needs, vital functions, chest drains, blood transfusion needs, duration of cardiopulmonary bypass, cross clamp time and anaesthesia time. The screening tests for neuropathic pain is the Douleur Neuropathique 4. Using at postopertative 3.month DN4 questionnaires predict persistent postoperative neuropathic pain.

Conditions

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Heart Surgery

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Patients included between 20-70 years
* ASA 1-4
* Euroscore value lower than 7
* Undergoned non coronary heart surgery (minithoracotomy and sternotomy)
* Intensive care has been discharged from the service in 24 hours , with patients given tramadol retard , metamizol, Dexketoprofen on postoperatif first day to discharged from the hospital.

Exclusion Criteria

* Diabetes mellitus
* Chronic renal failure
* COPD
* Uncontrolled hypertension
* Epilepsy
* Psychiatric disease
* Malignancy
* Patients with a history of cerebrovascular disease
* Patients with ischemia
* Patients suffering from chronic pain and analgesic use
* Patients taking antidepressants and antiepileptic drug
* Off-pump technique used or redo undergo cases
* Ongoing postoperative time thoracic or mediastinal drains more than 48 hours remaining patients, bleeding or patients who received repeated revisions due to infection
* More than 24 hours remaining in intensive care patients
* Patients with long discharge duration 1 week
* Patients who discontinued due to side effects of tramadol may begin after medicines.
* Postoperative wound infection.
Minimum Eligible Age

20 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Tobb University of Economics and Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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H. Evren Eker, Ass Prof

Role: STUDY_DIRECTOR

Baskent University Department of Anesthesiology

Other Identifiers

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2015-PMS-41

Identifier Type: -

Identifier Source: org_study_id

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