ClinicalTrials.gg
Not yet recruitingNCT06680024ICT and VATSUpdated Nov 8, 2024

Comparative Study Between Outcome of ICT Drainage and VATS in Management of Second Stage Empyema

An interventional study of Intercostal tube and Video assisted thoracoscope in Second Stage Empyema, sponsored by Sohag University. Not yet recruiting. Per ClinicalTrials.gov, last updated 2024-11-08.

Sponsored by Sohag University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2025, 1 year 3 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Sex
All
01

Study summary

The goal of this clinical trial is to compare between outcome of inter-costal tube drainage and video assisted thoracoscopic surgery in management of patients with second stage empyema.

It compares the outcome of both interventions in hospital stay, cost, wether need of decortication later on or not.

02

Conditions studied

  • Second Stage Empyema

Browse trials for

03

In context

Empyema

38 studies on the registry are indexed under Empyema; 11 are open to participants now.

This study's planned enrollment of 40 is below the median of 92 across 28 interventional studies indexed under Empyema.

Browse Empyema studies →

Lead sponsor

Sohag University is the lead sponsor of 1,230 studies on the registry; 636 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients both adults and children diagnosed as Empyema thoracis in early stages based on clinical examination, imaging modalities and pleural fluid analysis

Exclusion criteria

Exclusion Criteria:

  • Empyema due to carcinoma, terminally ill patients, patients with severe respiratory distress at admission, patients not fit for surgery, patients with co morbid diseases like cardiac disorders and .
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
40 participants (estimated)

Study arms

  • Active comparator
    Intercostal tube

    Intercostal tube as a primary intervention for treatment of second stage empyema

    Procedure: Intercostal tube

  • Active comparator
    Video assisted thoracoscope

    Video assisted thoracoscopic evacuation as a primary intervention for treatment of nd stage empyema

    Procedure: Video assisted thoracoscope

Interventions

  • ProcedureIntercostal tube

    Intercostal tube drainage as a first management of second stage empyema

    Also known as: Chest tube

  • ProcedureVideo assisted thoracoscope

    Video assisted thoracoscopic surgery as a first management for second stage empyema

    Also known as: VATS

06

What researchers measure

Primary outcomes

  1. the length of hospital stay

    Comparison between both intercostal tube drainage and video assisted thoracoscopic surgery in management of patients with second stage empyema, we will compare the length of hospital stay of each group of patients

    Time frame: From enrollment to 4 weeks

  2. cost of treatment of the patients' in each group

    Comparison between both intercostal tube drainage and video assisted thoracoscopic surgery in management of patients with second stage empyema, we will compare cost of treatment of the patients' in each group

    Time frame: 4 weeks

  3. number of participants with needs of decortication later on or not, assessed by the chest X-ray and CT chest.

    Comparison between both intercostal tube drainage and video assisted thoracoscopic surgery in management of patients with second stage empyema, we will compare with the chest X-ray and CT chest if there is residual empyema and whether the patients will need decortication later on or not

    Time frame: 4 weeks

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2024; primary completion for Jul 2025, 8 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 5, 2024
First posted
Nov 8, 2024
StartEst.
Nov 10, 2024
Primary completionEst.
Jul 30, 2025
CompletionEst.
Jul 31, 2025
Last update
Nov 8, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 8, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06680024
Lead sponsor
Sohag University
Responsible party
Mostafa Sayed Khalaf (Resident at cardiothoracic surgery department, sohag university hospitals, Sohag University) — Principal investigator
First posted
Nov 8, 2024
Start date
Nov 10, 2024 (estimated)
Primary completion
Jul 30, 2025 (estimated)
Completion
Jul 31, 2025 (estimated)
Last update
Nov 8, 2024

Study contacts

Mostafa Sayed Khalaf
Contact
Mostafasayed748@gmail.com
01027582257 ext. +20

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion