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OpenTrials
Completed

NCT Number: NCT05253014

Different Approaches for the Management of Post-dural Puncture Headache

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

Completed

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Key information

Age range

20 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Sohag faculty of medicine

Sohag, 82524, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The ASA physical condition І-П
  • 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

Treatment and study plan

Sphenopalatine Ganglion Block

Procedure

block of the sphenopalatine ganglion using either lidocaine or bupivacaine to relief postdural puncture headache

Paracetamol

Drug

intravenous paracetamol every 8 hours

Primary outcomes

  1. postdural puncture headache

    Time frame: within five days after the dural puncture

    visual analog scale

Sponsors and collaborators

Lead sponsor

Bahaa Mohammed Refaie

Other

Registry information

Official study title

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

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Feb 23, 2022
Registry last updated
Feb 23, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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