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Studying the effect of hypnosis on problems after nasal fracture surgery

Investigating the effect of preoperative hypnosis on complications and post-treatment problems in nasal fracture patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251108067916N1
Enrollment
26
Registered
2025-12-10
Start date
2026-01-08
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Patients with broken nose - hypnotizability - anxiety.

Interventions

Intervention 1: Intervention group: Hypnotic suggestions will be delivered by a hypnotist, consisting of verbal hypnotic suggestions followed by conditioned suggestions for postoperative analgesia. Hy

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: People who have suffered a nasal fracture with or without a septum Indications for Reconstruction should be closed. Indications for Reconstruction under sedation Have not previously undergone surgery with hypnosis Do not have psychiatric disorders Do not have chronic pain No use of opioid medications for more than 3 months

Exclusion criteria

Exclusion criteria: People who do not respond well to hypnosis during the study People who, for any reason, are unwilling to continue cooperation during the study.

Design outcomes

Primary

MeasureTime frame
Postoperative pain. Timepoint: The first patient assessment will be immediately after the patient leaves recovery. Subsequent assessments will be 3 hours, 6 hours, 12 hours, and 24 hours after leaving recovery. Method of measurement: visual analogue scale (from 0 to 10).

Secondary

MeasureTime frame
Anxiety. Timepoint: Immediately after recovery, 3 hours, 6 hours, 12 hours, and 24 hours after recovery. Method of measurement: visual analogue scale(0-10).;Nausea and vomiting. Timepoint: Immediately after recovery, 3 hours, 6 hours, 12 hours, and 24 hours after recovery. Method of measurement: visual analogue scale(0-10).;Dose of painkiller received. Timepoint: Immediately after recovery, 3 hours, 6 hours, 12 hours, and 24 hours after recovery. Method of measurement: Based on the amount of pain medication received after surgery in grams.;Patient satisfaction. Timepoint: Immediately after recovery, 3 hours, 6 hours, 12 hours, and 24 hours after recovery. Method of measurement: visual analogue scale(0-10).;Recovery period. Timepoint: after recovery. Method of measurement: Based on postoperative recovery time in minutes.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactkoorosh nematpour

Yazd University of Medical Sciences

koorosh19971375@gmail.com+98 35 3626 1990

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026