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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03156049 |
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Date of registration:
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14/05/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Sphenopalatine Ganglion Block Versus Occiptal Nerve Block in Treatment of Post Dural Puncture Headache
PDPH |
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Scientific title:
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Sphenopalatine Ganglion Block Versus Occiptal Nerve Block in Treatment of Postduarl Puncture Headache |
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Date of first enrolment:
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July 14, 2017 |
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Target sample size:
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93 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03156049 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Egypt
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Contacts
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Name:
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Hala Abdel-Ghaffar, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Assiut University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
ASA I-II Patients undergoing elective cesarean section requiring spinal anesthesia, who
developed PDPH during hospitalization or within days of the intrathecal block.
Exclusion Criteria:
- Patient refusal.
- Any contraindication to regional block (coagulopathy or anticoagulant therapy).
- Local scalp infection.
- Nasal polyp, trauma, septal deviation or any nasal pathology.
- Allergy to local anesthetics.
- Pregnancy induced hypertension.
- History of major psychiatric disorders.
- Chronic headache.
- Substance abuse.
- Current opioid use.
Age minimum:
18 Years
Age maximum:
45 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Headache
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Intervention(s)
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Procedure: Sphenopalatine block
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Procedure: Greater occipital nerve block
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Primary Outcome(s)
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Numeric rating pain score
[Time Frame: from intervention up to 24 hours]
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Secondary Outcome(s)
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Analgesic consumption
[Time Frame: from intervention up to 24 hours]
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Numeric rating pain score for headache.
[Time Frame: from intervention up to 24 hours]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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