A observational study to assess the effectiveness of sphenopalatine ganglion block and tb caffiene in treatment of Post dural pucture headache FOLLOWING lower segment ceaserean section

"A COMPARATIVE CLINICAL STUDY TO ASSESS THE EFFECTIVENESS OF SPHENOPALATINE GANGLION BLOCK AND ORAL CAFFEINE IN MANAGEMENT OF POSTDURAL PUNCTURE HEADACHE FOLLOWING LOWER SEGMENT CESAREAN SECTION".

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2022/10/046747

Enrollment

Registered

2022-10-25

Start date

Unknown

Completion date

Unknown

Last updated

2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Control Intervention1: TO assess the effectiveness of sphenopalatine ganglion block in managemnet of PDPH: To compare the effectiveness between sphenopalatine ganglion block and oral caffeine (300mg)

Eligibility

Inclusion criteria

Inclusion criteria: Patients who will give consent to participate in study patients aged between 18 yaear to 50 year female ASA physical grade 1 and 2

Exclusion criteria

Exclusion criteria: Patients refusal uncoperative patients history of facial trauma coagulopathy or bleeding diathesis

Design outcomes

Primary

Measure	Time frame
To evaluate the efficacy of sphenopalatine ganglion block in management of PDPH Timepoint: 24 week	—

Secondary

Measure	Time frame
To asess the side effect of sphenopalatine ganglion blockTimepoint: To assess the side effect of tablet caffeine;TO assess the efficacy of oral caffeine 300 mg in management of PDPH.Timepoint: 24 week	—

Countries

India

Contacts

Public ContactRajendra kumar

Gajra Raja medical college

drpreetiravigoyal@gmail.com9424455330

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026