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Perioperative Thoracotomy Analgesia; Different Analgesic Modalities

NCT ID: NCT04264689

Last Updated: 2020-12-07

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

Clinical Phase

NA

Total Enrollment

51 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-03-02

Study Completion Date

2020-11-03

Brief Summary

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the study aim is to compare the analgesic effect of thoracic epidural versus serratus plane block versus erector spinae block in thoracic surgeries

Detailed Description

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comparing the analgesic effect of thoracic epidural versus serratus plane block versus erector spinae block in thoracic surgeries regarding pain control and possible side effects

Conditions

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Analgesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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thoracic epidural

thoracic epidural will be done before induction of general anesthesia

Group Type ACTIVE_COMPARATOR

thoracic epidural

Intervention Type PROCEDURE

thoracic epidural

serratus anterior block

ultrasound guided serratus anterior block will be done after induction of general anesthesia

Group Type EXPERIMENTAL

serratus anterior block

Intervention Type PROCEDURE

ultrasound guided block

erector spinae block

ultrasound guided erector spinae block will be done after induction of general anesthesia

Group Type EXPERIMENTAL

erector spinae block

Intervention Type PROCEDURE

ultrasound guided block

Interventions

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serratus anterior block

ultrasound guided block

Intervention Type PROCEDURE

thoracic epidural

thoracic epidural

Intervention Type PROCEDURE

erector spinae block

ultrasound guided block

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* patients scheduled for thoracotomy age 18-65

Exclusion Criteria

* patient refusal coagulation defects abnormal kidney or liver functions local infection at site of block bone metastases
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute, Egypt

OTHER

Sponsor Role lead

Responsible Party

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Walaa Youssef Elsabeeny

lecturer of anesthesia and pain management

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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walaa Y elsabeeny, MD

Role: PRINCIPAL_INVESTIGATOR

Lecturer

Locations

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Department of anesthesia and pain medicine. National Cancer Institute

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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AP1906-50105

Identifier Type: -

Identifier Source: org_study_id