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Sphenopalatine Ganglion Block versus combined Ultrasound Guided Greater and Lesser Occipital Nerves Block for Management of Post Dural Puncture headache

Sphenopalatine Ganglion Block versus combined Ultrasound Guided Greater and Lesser Occipital Nerves Block for Management of Post Dural Puncture headache

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202505550555390
Enrollment
60
Registered
2025-05-14
Start date
2024-11-04
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Anaesthesia

Interventions

bilateral greater and lesser occipital nerves block

Sponsors

Faculty of Medicine menoufia univeristy
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients aged =18 years of both genders, of American Society of Anesthesiologists (ASA) physical status class I or II who have a history of spinal and/or epidural anesthesia complaining of headache not responding to conventional medical treatment and fulfilling the criteria of PDPH (fronto-occipital dull throbbing headache developing within 5 days of neuraxial block, exacerbated in upright position and is relieved by lying down, with any of the following associations neck stiffness, nausea, vomiting, dizziness, visual disturbances such as photophobia or diplopia, and/or auditory symptoms such as tinnitus). - Headache NRS =4 or modified lybecker score =2 on assuming upright position, whichever is present

Exclusion criteria

Exclusion criteria: • Patients who had recent nasal trauma, deformity, surgery or epistaxis. • Local infection • Patients with fever or coagulopathy. • Poor echogenic window hindering appropriate Trans Cranial Doppler examination. • Patients with cardiovascular, neuropsychiatric or cerebrovascular diseases • Opioid dependence. • Uncooperative patients. • Patient refusal. • Intellectual disabilities or those who cannot understand or report NRS. • Allergy to any drug used in the study

Design outcomes

Primary

MeasureTime frame
The primary outcome is the PDPH severity as assessed by NRS in upright position (for 15 minutes) 30 minutes after the block

Secondary

MeasureTime frame
Secondary outcomes include patient satisfaction, post block analgesic consumption, need to rescue block

Countries

Egypt

Contacts

Public ContactOla Saeed Mohammed

Lecturer of critical care medicine Faculty of Medicine Menoufia University

Ola.saeed@med.menofia.edu.eg02010011286684

Outcome results

None listed

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