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Sphenopalatine Ganglion Block For Post-Dural Puncture Headache In Obstetric Parturients

Sphenopalatine Ganglion Block For Post-Dural Puncture Headache In Obstetric Parturients: A Randomized Controlled Study - SPG Block for PDPH in Obstetric Parturients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042612
Enrollment
50
Registered
2022-05-18
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Health Condition 1: O745- Spinal and epidural anesthesia-induced headache during labor and delivery

Interventions

Intervention1: Sphenopalatine Ganglion Block: 1. The patient will be placed supine, with a folded sheet below both the shoulders and head in sniffing position. 2. Intervention â?¢ Two long cotton-ti

Sponsors

Sir Ganga Ram Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consenting obstetric parturients aged 18-45 years who receive neuraxial block for labour or caesarean delivery with development of PDPH within 72 h of dural puncture will be eligible to participate.

Exclusion criteria

Exclusion criteria: Parturient with chronic neurological disorder (epilepsy), bleeding disorder, allergy to local anaesthetics, deformity of the nasal septum, nasal polyps, frequent nosebleeds, those with nasal or sinus surgery within the past year or refusal to participate will be ineligible to participate

Design outcomes

Primary

MeasureTime frame
To assess efficacy of SPG block in terms of pain relief after PDPHTimepoint: 5min, 30 min, 2h, 4h, 8h,12h, 24h and 48 h

Secondary

MeasureTime frame
A. To observe at different time intervals 1) Pain relief in supine and sitting position 2) Numerical rating score (NRS) more than 3 in sitting position B. Time to first analgesic dose after the SPG block C. Relief in associated symptoms of PDPH (nausea, vomiting, visual changes, neck pain and stiffness) D. Presence of adverse effects (discomfort, change in taste, numbness in throat, epistaxis) associated with the block E. Need for epidural blood patch F. Parturient satisfaction Timepoint: 5min, 30 min, 2h, 4h, 8h,12h, 24h and 48 h

Countries

India

Contacts

Public ContactDr Anjeleena Kumar Gupta

Sir Ganga Ram Hospital

anjeleenasgrh@gmail.com9818422867

Outcome results

None listed

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