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THE PRACTICE OF BLOOD PATCH IN SPINAL SPACE FOR POST SPINAL PUNCTURE HEADACHE: A NATIONAL SURVEY

THE PRACTICE OF EPIDURAL BLOOD PATCH FOR POST DURAL PUNCTURE HEADACHE: A NATIONAL SURVEY

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/02/002414
Enrollment
500
Registered
2012-02-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Patients developing post dural puncture headache after spinal anaesthesia

Interventions

Intervention1: NIL: NIL Intervention2: Epidural blood patch: Under aseptic precautions patients own blood is injected into the epidural space with patient in lateral position Control Intervention1: Ep

Sponsors

Department of Anaesthesiology Pain and Perioperative Medicine Sir Ganga Ram Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Headache that develops less than seven days after a spinal puncture 2. Headache which occurs or worsens less than fifteen minutes after assuming the upright position, and improves less than thirty minutes in the recumbent position with at least one of the following (neck stiffness, tinnitus, hypacusia, photophobia, and nausea) 3. The headache should disappear within fourteen days after a spinal puncture

Exclusion criteria

Exclusion criteria: 1.Headache that develops more than seven days after a spinal puncture 2. Headache persisting for more than fourteen days

Design outcomes

Primary

MeasureTime frame
to evaluate the practice and utilisation of epidural blood patch as a treatment modality for post dural puncture headache in various institutions in our countryTimepoint: Headache starting within 7 days of dural puncture and lasting till 14 days

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr Nitin Sethi

Sir Ganga Ram Hospital

bimsharma@rediffmail.com09810135366

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026