Clinical Trials Directory

Trials / Completed

CompletedNCT05969119

Addition of Pyridostigmine to Conventional Management of Postdural Puncture Headache

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
All
Age
20 Years – 40 Years
Healthy volunteers
Accepted

Summary

Postdural puncture headache (PDPH) is a major complication of neuraxial anesthesia that can occur following spinal anesthesia and with inadvertent Dural puncture during epidural anesthesia. The presence of Pyridostigmine in CSF would be expected to increase the level of acetylcholine in CSF and subsequently in the brain through inhibition of cholinesterase. The increased level of acetylcholine would produce cerebral vasoconstriction.

Conditions

Interventions

TypeNameDescription
DRUGPyridostigmineParturients with postoperative Postdural puncture headache and a Visual analogue scale (VAS score) of ≥5 will receive either 60 mg oral Pyridostigmine every 6 hours or Placebo tablets similar in shape to pyridostigmine tablets every 6 hours.
DRUGPlaceboParturients with postoperative Postdural puncture headache and a Visual analogue scale (VAS score) of ≥5 will receive Placebo tablets similar in shape to pyridostigmine tablets every 6 hours.

Timeline

Start date
2023-07-25
Primary completion
2024-01-03
Completion
2024-01-03
First posted
2023-08-01
Last updated
2024-09-04

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05969119. Inclusion in this directory is not an endorsement.