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NCT05253014 Clinical Trial

Different Approaches for the Management of Post-dural Puncture Headache

Post-Dural Puncture Headache Clinical Trial

Official title:
Comparative Study Between Different Approaches for the Management of Post-dural Puncture Headache

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05253014
Other study ID # 2223
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2018
Est. completion date December 30, 2020

Study information
Verified date February 2022
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Detecting the efficacy and safety of trans-nasal sphenopalatine ganglion block using either lidocaine 2% or bupivacaine 0.5 % as a treatment line for post-dural puncture headache

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date December 30, 2020
Est. primary completion date October 30, 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: - The ASA physical condition ?-? - the patient underwent CS under spinal anesthesia - The headache developed within 5 days after the dural puncture - There is no different explanation for the headache Exclusion Criteria: - coagulopathy - history of nasal bleeding - nasal polyp - septal deviation - local anesthetics reaction

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• sphenopalatine ganglion block
block of the sphenopalatine ganglion using either lidocaine or bupivacaine to relief postdural puncture headache
Drug:
• paracetamol
intravenous paracetamol every 8 hours

Locations
Country Name City State
Egypt Sohag faculty of medicine Sohag

Sponsors (1)
Lead Sponsor Collaborator
Bahaa Mohammed Refaie

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary postdural puncture headache visual analog scale within five days after the dural puncture
See also
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Terminated NCT02813655 - Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE) Phase 2
Completed NCT02522013 - Aminophylline for Patients With Post-Dural Puncture Headache Phase 3
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Completed NCT05262933 - Effects of Preoperative Coffee Consumption in Cesarean Sections Under Spinal Anesthesia
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Completed NCT00370604 - Effect of Small Versus Large Epidural Needles on Postdural Puncture Headache Study N/A
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Withdrawn NCT03560349 - RCT of SPG Blocks for Post-dural Headache Phase 2
Recruiting NCT06253754 - Pathophysiological Mechanisms and Implication of Treatment in Postural Puncture Headache