Clinical Trials Directory

Trials / Completed

CompletedNCT04793490

Sphenopalatine Ganglion Block for Management of Post- Dural Puncture Headache in Obstetric Patients

Efficacy and Efficiency of Sphenopalatine Ganglion Block for Management of Post-dural Puncture Headache in Obstetric Patients-A Randomized Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
21 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The purpose of this trial is to study the efficacy and efficiency of sphenopalatine ganglion block for management of post dural puncture headache in obstetric patients

Detailed description

Background and objectives: Post dural puncture headache(PDPH) is a common complication of lumbar puncture, it is likely due to the loss of cerebrospinal fluid into the epidural space through the dural tear. The prevalence of PDPH is higher in pregnant women.Sphenopalatine ganglion block (SPGB) is a non-invasive intervention with minimal adverse effects, it is indicated in acute and chronic facial/head pain like cluster headache, trigeminal neuralgia, post herpetic neuralgia and pain due to head and neck cancer.SPGB can be performed by different approaches:transnasal,transoral ,sub zygomatic and lateral infratemporal.Transnasal is the easiest, least invasive approach which can be done at bedside. The objective of this trial is to study the efficacy and efficiency of sphenopalatine ganglion block for management of post-dural puncture headache in obstetric patients.The following will be recorded: pain score will be assessed using the numeric rating pain scale(NRS),heart rate and mean arterial pressure, onset and duration of analgesia, total dose of ketorolac, duration of hospital stay and patient satisfaction

Conditions

Interventions

TypeNameDescription
PROCEDURESphenopalatine ganglion blockPatients will receive the SPGB via the transnasal approache by a cotton tipped applicator soaked in lignocaine 2% with 4 mg dexamethasone
DRUGparacetamolpatients will receive paracetamol 1 g thrice daily intravenously

Timeline

Start date
2021-03-15
Primary completion
2021-11-25
Completion
2021-12-05
First posted
2021-03-11
Last updated
2022-02-16

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04793490. Inclusion in this directory is not an endorsement.