Suspended

pigtailPigtail Catheter for Drainage of (Pneumothorax/Simple Effusion) is a Effective Procedure

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Pleural Diseases

+ Pleural Effusion

+ Respiratory Tract Diseases

From 18 to 65 Years
+5 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: December 2022
See protocol details

Summary

Principal SponsorAssiut University
Study Contactmohamed g gaber, residentMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 2022

Actual date on which the first participant was enrolled.

Chest injuries are common following blunt and penetrating trauma. Fewer than 10 per cent of blunt injuries and 15-30 per cent of penetrating injuries require surgical management1. Most can be managed with tube thoracostomy to expand the lung (pneumothorax) or to drain blood (haemothorax)2. Although tube thoracostomy is fairly effective, it can be associated with complications such as mispositioning, malfunction, or injury by insertion through the diaphragm or liver3-5. The standard tube size. Has usuallybeen32-40Fr.Insertion of such a large -calibre tube requires a cut-down technique, can be traumatic, and is often associated with significant pain and discomfort. Pigtail catheters, originally used by cardiologists to drain chronic pericardial effusion6, were later modified and adapted for pleural drainage7. Because of their small size and reduced trauma during placement, patients may experience significantly decreased pain and discomfort. Pigtail catheters are frequently used in the paediatric population8-10, as well as in adult, non-traumatic situations11-17 Pigtail catheters inserted at the bedside have similar efficacy to traditional chest tube.

Official TitlePigtail Catheter for Drainage of (Pneumothorax/Simple Effusion) is a Effective Procedure
NCT05641779
Principal SponsorAssiut University
Study Contactmohamed g gaber, residentMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

25 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Pleural DiseasesPleural EffusionRespiratory Tract Diseases

Criteria

1 inclusion criteria required to participate
iatrogenic pneumothorax

4 exclusion criteria prevent from participating
Age less than 18 years.

refused to participate.

Unconscious.

spontaneous pneumothorax.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Assiut University Hospital

Asyut, EgyptOpen Assiut University Hospital in Google Maps
SuspendedOne Study Center