A randomized control study to assess the efficacy of sphenopalatine ganglion block in patients with postdural puncture headache

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

PACTR

Registry ID

PACTR202401546543440

Enrollment

Registered

2024-01-04

Start date

2023-09-05

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Anaesthesia

Interventions

group B

Group A

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: patients suffering from postdural puncture headache after spinal anesthesia not responding to usual reatment

Exclusion criteria

Exclusion criteria: patients with coagulopathy.,nasal septum deviation ,polyp, history of nasal bleeding and allergy to local anesthetics

Design outcomes

Primary

Measure	Time frame
pain intensity in upright position	—

Secondary

Measure	Time frame
frequency of analgesia taken	—

Countries

Egypt

Contacts

Public ContactAhmed Mostafa

professor of anesthesia

basaahmed@yahoo.com00201005204130

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026