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Comparing different doses of Bupivacaine in spinal anesthesia in anal surgeries

Comparative study of Bupivacaine different doses in spinal anesthesia in anal surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138901213562N1
Enrollment
70
Registered
2010-04-10
Start date
2009-08-15
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

spinal anesthesia. complications of surgical and medical care, not elsewhere classified

Interventions

Intervention 1: Group A: 2mg of Bupivacaine 0.5% hyperbaric was injected by 24 gaguge Quincke spinal needle in L4,L5 space in sitting position. Intervention 2: Group B: 5mg of Bupivacaine 0.5% hyperba
Treatment - Drugs
Group A: 2mg of Bupivacaine 0.5% hyperbaric was injected by 24 gaguge Quincke spinal needle in L4,L5 space in sitting position.
Group B: 5mg of Bupivacaine 0.5% hyperbaric was injected by 24 gaguge Quincke spinal needle in L4,L5 space in sitting position.

Sponsors

Private
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients who were candidate for elective anal surgeries with ASA I or II. Exclusion criteria: patients who had pain and did not answer to injecting 1cc of Fentanyl or the ones who their surgery took more than 15 min.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain degree. Timepoint: after performing spinal anesthesia and during surgery. Method of measurement: Mc-Gill quesionnaire and VAS method.

Secondary

MeasureTime frame
Ability to walk and finishing the block of S4 dermatom. Timepoint: after finishing the surgery. Method of measurement: VAS, clinician examination and direct interview with patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Khosro Farhadi

Kermanshah University of Medical Sciences

kh-farhadi@kums.ac.ir+98 83 1428 2670

Outcome results

None listed

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