About Pricing FAQs Blog

Loading clinical trials...

Your health journey, clearly organized.

Find Clinical Trials →

Legal

Privacy Policy
Terms of Service

© 2026 Clareo Health. All rights reserved.

Back to clinical trial search

COMPLETEDNANCT04401878

SGB in Management of Patients With PDPH Using TCD

This study aims to investigate the ability of SPGB in the management of PDPH. Transcranial Doppler is also used as an measure to assess the block success by detecting the variability in the cerebral h...

Lead sponsor: Zagazig University•1 locations•View source on ClinicalTrials.gov

Clareo plain-language summary

What this study is about

Generating AI summary...

Save this trial guide to your notes

Keep your clinical trial research organized — questions to ask, what to expect, and key details.

Sponsors

Lead Sponsor

Zagazig University

This clinical trial is performed in postoperative orthopedic unit. In this study, 120 patients were enrolled who had an epidural anesthesia; 60 patients who developed PDPH joined the treatment group (A) and received the SP block. They are assessed before the procedure by NRS and at 30 mins, 2h, 4h, 6h, 12h, and 24h after the procedure. Patients are also assessed by TCD before and after the block. The control group (B) included 60 patients with no PDPH.

Age

18 - 60 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•patients are considered who had an epidural anesthesia
•Patients with ASA 1 and 2
•Patients' age ranged from 18 to 60 years.

Exclusion Criteria

•Patients with septal perforation, nasal septum deviation,or nasal bleeding.
•Patients have recent nasal trauma
•Patients have recent nasal surgery
•Patients have a nasal infection
•Patients within ASA 3 and 4
•Patients older than sixty yrs or younger than eighteen yrs.

Related studies

Contribution of Ondansetron to Preventing Post-Dural Puncture Headaches Following Spinal Anesthesia

NCT06444737 · Post-Dural Puncture Headache

Active Not Recruiting

Factors Associated With the Onset of Chronic Headaches in Patients Who Received a Blood Patch in Post Partum

NCT05888324 · Blood Patch, Post-Dural Puncture Headache

Not Yet RecruitingNA

Comparison of Post-Dural Puncture Headache After Spinal Anesthesia Using Median Versus Paramedian Approach

NCT07436403 · Post-Dural Puncture Headache, Headache After Spinal Puncture

TERMINATEDPhase 2

Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE)

NCT02813655 · Post-dural Puncture Headache

Nebulized Dexmedetomidine Versus Oral Sumatriptan in Treatment of Post Dural Puncture Headache in Cesarean Section

NCT06514040 · Post-Dural Puncture Headache

View all related studies →

Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: July 22, 2021Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment120

Start dateMay 2020

Last updatedJul 22, 2021

Condition

Post-Dural Puncture Headache

Locations shown

Faculty of Medicine, Zagazig University

Zagazig

For caregivers

Use Clareo to keep notes, questions, trial details, and next steps organized before and after appointments.

Start free trial →

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: July 22, 2021Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions