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Comparison of Sprotte and Quincke needles with respect to post dural puncture headache

Comparison of Sprotte and Quincke needles with respect to post dural puncture headache

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201009292080N4
Enrollment
162
Registered
2010-12-28
Start date
2010-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

headache. Other specified headache syndromes

Interventions

Sprotte spinal needle
Quincke spinal needle
Intervention 1: Sprotte spinal needle. Intervention 2: Quincke spinal needle.
Treatment - Devices

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 16- 65, patients with major surgery of lower limb or lower abdominal segment under spinal anesthesia. Exclusion criteria: patients with chronic headache and drug induced headache.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache. Timepoint: every 4 hours till 24 hours after surgery. Method of measurement: checklist and physical exam.

Secondary

MeasureTime frame
Tinnitus. Timepoint: every 4 hours till 24 hours after surgery. Method of measurement: checklist & physical exam.;Hypotension. Timepoint: every 4 hours till 24 hours after surgery. Method of measurement: checklist & physical exam.;Vertigo. Timepoint: every 4 hours till 24 hours after surgery. Method of measurement: checklist & physical exam.;Nausea & vomitting. Timepoint: every 4 hours till 24 hours after surgery. Method of measurement: checklist & physical exam.;Nuchal rigidity. Timepoint: every 4 hours till 24 hours after surgery. Method of measurement: checklist & physical exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfsane Norouzi

Arak University of Medical Sciences

norouzi.a@arakmu.ac.ir+98 86122247900

Outcome results

None listed

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