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NCT05116930

Neostigmine and Glycopyrrolate for the Treatment of Post Dural Puncture Headache After Known Dural Puncture With a Tuohy Needle: A Pilot Study

Recruiting now Phase 2 Last updated 18 March 2026
What this trial tests

Phase 2 trial testing Neostigmine in Post-Dural Puncture Headache in 18 participants. Currently enrolling.

Timeline
19 November 2021
Primary endpoint
1 December 2027
1 December 2027

Quick facts

Lead sponsorMayo Clinic
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment18
Start date19 November 2021
Primary completion1 December 2027
Estimated completion1 December 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Mayo Clinic

Who can join

Adults 18 to 54, female only, with Post-Dural Puncture Headache. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to evaluate Neostigmine and Glycopyrrolate to treat post-dural puncture headache (PDPH) to reduce the proportion of postpartum women with a PDPH requiring epidural blood patch (EBP) who developed a PDPH after accidental dural puncture.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Neostigmine

Trials testing the same drug.

Other recruiting trials for Post-Dural Puncture Headache

Currently open trials in the same condition.

Other Mayo Clinic trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05116930.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing