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Which brain surgery method works best for blood clot removal?

NCT ID NCT07368101

Disease control Sponsor: Services Institute of Medical Sciences, Pakistan Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 60 adults with chronic subdural hematoma (a blood clot on the brain) to see if using one or two small holes in the skull (burr holes) leads to better recovery. The goal was to find which method reduces complications like infection, clot return, and hospital stay. Participants were split into two groups, each receiving one of the surgical techniques, and followed for three months after surgery.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

60 people

The number who actually took part.

Started

Oct 2024

Finished

May 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

20 to 70 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients aged 20-70 years both genders diagnosed with subdural hematoma Exclusion Criteria: * • Patients in shock (BP≤100/60 mmHg) or history of seizures * Patients with bleeding disorder (PT\>15 sec) or intake of anti-coagulants * Patients undergoing or already had ventriculoperitoneal shunt * Patients with epilepsy, or obsessive compulsive decoder * Patients with already operated for subdural hematoma * Patients with post-cerebrospinal fluid diversion subdural hematoma

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Conditions

The condition(s) this trial relates to.

Hematoma, Subdural, Chronic

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Chronic subdural hematoma

Contacts and locations

Locations

  • Services Institute of Medical Sciences / Services Hospital

    Lahore, Punjab Province, 54770, Pakistan

More trials for these conditions

Other studies related to the condition(s) this trial covers.