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Comparison of the effect of adding Neostigmine to Ropivacaine and sufentanilto Ropivacaine in spinal anesthesia for herniorrhaphy surgery

Comparison of the effect of adding Neostigmine to Ropivacaine and sufentanilto Ropivacaine in spinal anesthesia for herniorrhaphy surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141209020258N107
Enrollment
105
Registered
2019-04-23
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-05-21

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

Conditions

Spinal anesthesia. Intentional self-poisoning by and exposure to other and unspecified drugs, medicaments and biological substances

Interventions

Intervention 1: Intervention group: We inject 3 milliliter of Ropivacaine(15 milligram) plus 50 micro gram Neostigmine (Caspian.Co.Rasht)(1 milliliter) in form of intrathecal. Intervention 2: Interven

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 18 to 60 years Patients candidate inguinal hernia surgery Lack of cardiovascular problems Absence of coagulation disorders Lack of peripheral and central neuropathy No history of allergy to Neostigmine and Ropivacaine and Sufentanil Non-localized infection in the spinal cord

Exclusion criteria

Exclusion criteria: Patient dissatisfaction Failure to perform spinal anesthesia

Design outcomes

Primary

MeasureTime frame
Mean arterial blood pressure. Timepoint: Every 15 minutes during surgery and recovery time and up to 2 hours after surgery. Method of measurement: Barometer.;Heart rate. Timepoint: Every 15 minutes during surgery and recovery time and up to 2 hours after surgery. Method of measurement: Count.;Percent of oxygen saturation. Timepoint: Every 15 minutes during surgery and recovery time and up to 2 hours after surgery. Method of measurement: Pulse oximetry.;Duration of motor block. Timepoint: Every 5 minute. Method of measurement: Minute.;Duration of Sensory block. Timepoint: Every 1minute. Method of measurement: Minute.;Pain. Timepoint: Recovery and 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale Questionnaire.;Mean of narcotic. Timepoint: 24 hour after surgery. Method of measurement: Milligram.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alireza Kamali

Arak University of Medical Sciences

alikamaliir@yahoo.com+98 86 3222 2003

Outcome results

None listed

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