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OpenTrials
Completed

NCT Number: NCT04264689

Perioperative Thoracotomy Analgesia; Different Analgesic Modalities

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

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of anesthesia and pain medicine. National Cancer Institute

Cairo, 11796, Egypt

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

serratus anterior block

Procedure

ultrasound guided block

Thoracic Epidural

Procedure

thoracic epidural

erector spinae block

Procedure

ultrasound guided block

Primary outcomes

  1. visual analogue score

    Time frame: 24 hours

    minimum value 0 and maximum value 10

Secondary outcomes

  1. mean arterial blood pressure

    Time frame: 24 hours

    measurement of mean arterial blood pressure

Sponsors and collaborators

Lead sponsor

National Cancer Institute, Egypt

Other

Registry information

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Feb 11, 2020
Registry last updated
Dec 7, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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