The Evaluation of Postoperative Pain After Caesarean Section

NCT ID: NCT02332395

Last Updated: 2017-04-19

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

COMPLETED

Total Enrollment

115 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-12-31

Study Completion Date

2016-05-31

Brief Summary

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The aim of this study is to determine the effect of surgical priority either emergency or elective on postoperative pain in caesarean section operations. Patients whose undergo caesarean section operation are included into this study. Patients will invite to complete the Pain Catastrophizing Scale questionnaire in preoperative period. The patients will be divided into two groups in terms of applied surgical priority whether emergency or elective. After caesarean section, patient controlled analgesia is used for pain relief. And the intensity of pain will be measured by using numerical rating scale.

Detailed Description

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Pain is the main problem of postoperative period. Postoperative analgesic consumption can be associated with physical and psychological condition of the individual. This study is aimed to investigate the effect of surgical priority either emergency or elective on postoperative pain in caesarean section operations.

Patients are invited to complete the pain catastrophizing scale questionnaire in preoperative period.

A total of 100 patients will be included into the study. Patients are divided into two groups in terms of surgical priority whether emergency or elective. Spinal or general anesthesia will be performed to the patients. In postoperative period, patient controlled analgesia will be applied for pain relief and numerical rating scale is used to determine the pain intensity in 1st, 2nd, 6th, 12th, 24th hours. The analgesic consumption in 24 hours will be recorded.

Conditions

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Pain

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Emergency caesarean section

patients whose underwent emergency caesarean section operation

No interventions assigned to this group

Elective caesarean section

patients whose underwent elective caesarean section operation

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* American Society of Anesthesiologists score of 1 or 3 and 1-Emergency or 3-Emergency

Exclusion Criteria

* Patients whose not to participate
* Patients whose have communication problems
* Patients whose have been using antipsychotic or antidepressant drugs
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Tokat Gaziosmanpasa University

OTHER

Sponsor Role lead

Responsible Party

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Hakan Tapar

Assistant Professor, MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Hakan Tapar, Ass.Prof, MD

Role: PRINCIPAL_INVESTIGATOR

Gaziosmanpasa University, Medical Faculty, Department of Anesthesiology and Reanimation

Locations

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Gaziosmanpasa University

Tokat Province, Tokat Province, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Taşdemir A, Erakgün A, Nuri Deniz M, ÇertuğA . Preoperatif Bilgilendirme Yapılan Hastalarda Ameliyat öncesi ve Sonrası Anksiyete Düzeylerinin State-Trait Anxiety Inventory Test ile Karşılaştırılması. Turkish Journal Anaesthesiology and Reanimation 41(2): 44-9, 2013.

Reference Type BACKGROUND

Kırdemir P, Özorak Ö. Postoperatif Ağrı ve Analjezik İhtiyacı Preoperatif Dönemde Tahmin Edilebilir mi? Turkiye Klinikleri Journal of Medical Sciences 31(4):951-9, 2011.

Reference Type BACKGROUND

Hüseyinoğlu Ü, Ülker K, Temur İ, Kütük M. Elektif Sezaryen Doğum Sonrası Postoperatif Ağrı Gideriminde Meperidin ve Tramadolün Karșılaștırılması: Bir Prospektif Randomize Çalıșma. Kafkas Journal of Medical Sciences 1(2):53-56, 2011.

Reference Type BACKGROUND

Other Identifiers

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13-KAEK-226

Identifier Type: -

Identifier Source: org_study_id

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