CClinicalTrials.gg
Status unknownNCT05792683Updated Mar 31, 2023

Comparison of Duration of CSF Leak in Post Traumatic Patients Managed by Early Lumbar Drain vs Conservative Treatment

An interventional study of lumbar drain in CSF Leakage, sponsored by Rawalpindi Medical College. Status unknown at 1 site in Pakistan. Open to participants aged 15 Years to 60 Years. Per ClinicalTrials.gov, last updated 2023-03-31.

Sponsored by Rawalpindi Medical College · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2023), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
15 Years to 60 Years
Sex
All
01

Study summary

As limited data is available locally and internationally regarding early Lumbar drain and its effect on duration of CSF leak we have decided to compare it conservative treatment. By providing CSF an alternative route for drainage, the fistula site will remain dry. Leakage site won't be facing CSF pressure, and this will promote early healing of the wound.

Read the detailed description

Cerebrospinal fluid (CSF)leak is caused by communication between the subarachnoid space and the air-filled spaces of the middle ear or para nasal sinuses and sometimes skin. CSF leaks can be divided into two types ,traumatic and non traumatic. The traumatic CSF leaks further divided into accidental and iatrogenic (post surgical procedures) 1. Almost 80% of CSF leaks are due to road traffic accidents, fall from heights and firearms injuries to brain and spine, 16% are iatrogenic, and 4% are non-traumatic 1,2. More than 50% of traumatic CSF leaks are evident within the first 02 days, 70% within the first week, and almost all present within the first 3 months [2,3]. It is estimated that in patients with skull base fracture 10-30% develops CSF leaks and 2% of all traumatic head injuries are associated with CSF leaks [4].With the help of conservative treatment most of the CSF leaks stop within 7-10 days 1,5. When the CSF leak doesn't stop after 7-10 days, a lumbar drainage (LD) is suggested3,7. LD(lumbar drain) is a recommended treatment method for the CSF leaks in skull base and spinal trauma, the indications for LD(lumbar drain ) placement are still controversial ,LD(lumbar drain) effect on early CSF leakage cessation is still arguable 2,3. Traumatic CSF leaks duration can be reduced by early( lumbar drain) placement . At tertiary level particularly in public hospital, our study will be helpful to document the benefits of early lumbar drain (LD) in traumatic CSF leakage patients and their hospital stay. This will also help to reduce the ambiguity regarding the protocol for early lumbar drain (LD) placement .

02

Conditions studied

  • CSF Leakage
03

In context

Cerebrospinal Fluid Leak

45 studies on the registry are indexed under Cerebrospinal Fluid Leak; 10 are open to participants now.

This study's planned enrollment of 60 is below the median of 68 across 27 interventional studies indexed under Cerebrospinal Fluid Leak.

Browse Cerebrospinal Fluid Leak studies →

Lead sponsor

Rawalpindi Medical College is the lead sponsor of 22 studies on the registry; 5 are open to participants now.

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

04

Who can participate

Ages eligible
15 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Age between 15-60 years in both genders.
  2. Patients with craniospinal post traumatic or post operative CSF leakage for more than 24 hours.

Exclusion criteria

Exclusion Criteria:

  1. Patients with comorbid like Cardiovascular, Chronic Kidney Disease, Coagulopathies and Pregnancy
  2. Previous history of chest or abdominal surgery.
  3. Previous history of any lumbosacral surgery.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Early lumbar drain

    30 in this group

    Device: lumbar drain

  • Other
    conservative treatment

    30 in this group

    Device: lumbar drain

Interventions

  • Devicelumbar drain

    Patient will be placed in the lateral decubitus position; catheter will be inserted by using a Tuohy needle in the interspinous area of lumbar spine. The LD catheter will reach the lumbar subarachnoid space.The remaining part of the drainage kit will be placed along the back of the patient. The catheter insertion site will be sutured and treated with povidone-iodine ointment. Sterile drape will be used to cover the entire external part of the LD. The CSF will be collected within the closed beg. CSF drainage through LD will be around 10 ml per hour or 200-250 ml/day.

06

What researchers measure

Primary outcomes

  1. Length of active CSF leak in post-traumatic patients with Lumbar drain.

    Lumbar drain will reduce the CSF pressure on the wound which will lead to early healing of CSF leak sight.it will reduce the duration of CSF leak in post traumatic patients .

    Time frame: 06 months

Secondary outcomes

  1. incidence of recurrence of CSF leaks, meningitis after treatment

    After treatment with both methods the incidence of recurrence of CSF leaks and meningitis will be recorded .

    Time frame: with in 06 months

07

Study locations

1 of 1 sites recruiting
  • RMU
    Rawalpindi, Punjab 4600, Pakistan
    • Atiq UR rehman, MBBS · Contact · drnehria@gmail.com · 00923344314213
    • Atiq UR [arehman] · Contact
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — Results of study

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 31, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05792683
Lead sponsor
Rawalpindi Medical College
Responsible party
Dr Atiq ur Rehman (dr atiq, Rawalpindi Medical College) — Principal investigator
First posted
Mar 31, 2023
Start date
Feb 21, 2023
Primary completion
Jul 21, 2023 (estimated)
Completion
Aug 21, 2023 (estimated)
Last update
Mar 31, 2023

Study contacts

Atiq UR [arehman], MBBS
Contact
drnehria@gmail.com
00923344314213
Atiq UR [arehman]
principal investigator · Rawalpindi Medical College

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2023. You cannot join it, but the record below documents what was studied.

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