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Relevance analgesia and side effects with Fentanyl epidural and Fentanyl, Bupivacaine epidural after spinal surgery

Comparison of analgesia and side effects in Fentanyl epidural and Fentanyl, Bupivacaine epidural after spinal surgery Spondylolisthesis surgery and Spinal fixation Spondylolisthesis surgery and Spinal fixation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014031016917N1
Enrollment
90
Registered
2014-06-27
Start date
2014-07-23
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

Relevance analgesia and side effects with Fentanyl epidural and Fentanyl - Bupivacaine epidural after spinal surgery.

Interventions

Intervention 1: Intervention 1) For primary pain control Apotel 1 gram in 100 cc normal saline will be infused 20 minutes prior to the end of surgery, then repeat every 6 hours. . If VAS is more tha
Treatment - Drugs
Prevention
Intervention 1) For primary pain control Apotel 1 gram in 100 cc normal saline will be infused 20 minutes prior to the end of surgery, then repeat every 6 hours. . If VAS is more than 4 , we inject
Intervention 2) Surgeon put an epidural catheter in the L3-L4 epidural space at the end of operation. Epidural pump with 100 microgram Fentanyl added to 98 cc normal saline 3–5 ml/h after patient arri
Intervention3) The Surgeon put an epidural catheter in the L3-L4 epidural space at the end of operation. Epidural pump with 98 cc normal saline add to100 microgram Fentanyl and Bupivacaine 0.125 %( 24

Sponsors

Vice chancellor for research of Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients aged 18 to 75 years old; patients undergoing Spondylolisthesis surgery and Spinal fixation;American Society of Anesthesiologists (ASA) I, II, III Exclusion criteria: If the Dural be damaged; Patient dissatisfaction

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: when patient were transferred to the section from recovery unit then every 6 hours to 24 hours. Method of measurement: Visual analogous score.;Hypotension. Timepoint: when patient were transferred to the section from recovery unit then every 6 hours to 24 hours. Method of measurement: mmHg, Saadat company.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli ashraf

Guilan University of Medical Sciences

arcguilan1392@gmail.com; alishraf@yahoo.fr+98 13 1321 0434

Outcome results

None listed

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