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Comparison of Sprotte and Quincke spinal needles on the frequency of spinal anesthesia failure

Comparison of Sprotte and Quincke spinal needles on the frequency of spinal anesthesia failure in patients undergoing cesarean delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110712007013N25
Enrollment
100
Registered
2019-12-21
Start date
2019-07-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Frequency of spinal anesthesia failure. Other complications of spinal and epidural anesthesia during labor and delivery

Interventions

Intervention 1: Intervention group: The patients of study group (n=50) using of Sprotte( manufacturer: B brown) spinal needle G25 undergoing spinal anesthesia. Intervention 2: Control group: The pat

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Candidate for elective cesarean delivery Candidate for spinal anesthesia Aged 18-40 years ASA Class I&II Term and singleton pregnancy

Exclusion criteria

Exclusion criteria: Weight over 100 kg and height less than 150 cm Allergy to local anesthetics History of psychiatric disease History of systemic diseases (cardiovascular, hepatic, pulmonary, ...) Spinal cord stenosis and lumbar discopathy

Design outcomes

Primary

MeasureTime frame
Frequency of “overall failure“ of spinal block. Timepoint: At the beginning of the intervention and in 5th,10th and 15th minutes after the intervention. Method of measurement: Cold sensation.;Frequency of partial failure“ of spinal block. Timepoint: At the beginning of the intervention and in 5th,10th and 15th minutes after the intervention. Method of measurement: Cold sensation.

Secondary

MeasureTime frame
Postoperative side effects related to spinal anesthesia. Timepoint: Post anesthesia care unite, and during 24 hours postoperatively. Method of measurement: Observational.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Simin Atashkhoyi

Tabriz University of Medical Sciences

satashkhoyi@gmail.com+98 41 3553 9161

Outcome results

None listed

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