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Efficacy Assessment of Two Methods for Pain Management Following Anorectal Surgery

Clinical Trial of Efficacy Assessment of Patient Controlled Analgesia vs. Pudendal Nerve Block for Pain Management Following Anorectal Surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016100515640N4
Enrollment
100
Registered
2016-10-23
Start date
2012-03-01
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

Anorectal Disease. Disease of anus and rectum, unspecified

Interventions

Intervention 1: In pudendal nerve block group, 5 milliliter marcaine 0.5% diluted with normal saline to reach the volume of 8cc administered in clock 3 and 9 of perianal area. The patients’ pain score
Treatment - Drugs
In pudendal nerve block group, 5 milliliter marcaine 0.5% diluted with normal saline to reach the volume of 8cc administered in clock 3 and 9 of perianal area. The patients’ pain score were checked ev
In patient controlled analgesia group, patients connected to a pomp containing 20 mg morphine sulphate diluted in 100 cc normal saline adjusted infusion rate at 4cc/hour and 1cc for bolus every 15 min

Sponsors

Vice chancellor for research, Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients with American Society of Anesthesiologists (ASA) Class I or II; candidate for elective anorectal surgery under general anesthesia Exclusion Criteria: Pregnancy; opium addiction; documented cardiovascular or pulmonary disease; allergy to the drugs using in trial

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 0, 6, 12, 24 hours after surgery. Method of measurement: Numerical Rating Scale (NRS).;Patient Satisfaction. Timepoint: Until 24 hours after surgery. Method of measurement: Numerical Rating Scale (NRS).

Secondary

MeasureTime frame
Side effects. Timepoint: Until 24 hours after surgery. Method of measurement: Serial physical exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Alireza Baratloo

Shahid Beheshti University of Medical Sciences

alirezabaratloo@yahoo.com+98 21 2272 1155

Outcome results

None listed

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