Health Condition 1: 8- Other Procedures
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients giving consent . Patients in ASA Grade 1,2,3 Pateints within 5 days of dural puncture Patients returning to OPD with symptoms of PDPH after discharge
Exclusion criteria
Exclusion criteria: Patients not giving consent Patients with chronic headache, tension headache, migraine, Cluster headache. Patients with known nasal septal deviation or abnormalities such as polyps, intranasal tumors Patients with a history of any disorders involving the nose such as sinusitis, rhinitis Patients with a history of allergy to study medications (Lignocaine or Dexmedetomidine or paracetamol ) Patients on analgesic or undergoing treatment for headache. Patients with a history of addiction i.e. alcohol abuse or substance abuse.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome of the study is to assess the Efficacy of SPGB for the treatment of PDPH and conservative management assessed by reduction in pain scoreTimepoint: Outcomes wil be assessed at baseline 15mins 30mins 1 hour 2 hours 6hours 12 hours 24hours 48 hours 72hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome of the study is to assess the Efficiency of the Sphenopalatine block & conservative management by the assessment of onset & duration of analgesia, as well as the development of any side effects associated with block , total dose of rescue analgesia & hospital discharge & patient satisfaction.Timepoint: Outcomes will be assessed at Baseline 15mins 30mins 1 hour 2 hours 6 hours 12 hours 24 hours 48 hours 72 hours | — |
Countries
India
Contacts
Ganesh Shankar vidyarthi memorial medical college