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BEnefit of HYpnosis on Pain During Stitches in Emergency Room

BEnefit of HYpnosis on Pain During Stitches in Emergency Room: The BE-HYPER Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06497712
Acronym
BE-HYPER
Enrollment
180
Registered
2024-07-12
Start date
2025-05-15
Completion date
2028-05-15
Last updated
2026-06-02

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

Conditions

Wound of Skin

Keywords

hypnosis, wound, stitches, pain, sinusal variability of cardiac frequency

Brief summary

Suturing is a daily practice in the emergency department, but it can be painful and stressful for patients. Hypnosis is increasingly used as a complement to the usual painkillers. The aim of our study was to investigate the impact of hypnosis on stitch placement in emergency department patients presenting with lacerations assessed by heart rate variability.

Detailed description

The aim of this randomized, controlled, single-center, prospective study is to evaluate the impact of hypnosis during stitching in emergency department patients presenting with a laceration assessed by heart rate variability. All patients with eligibility criteria will be included if the patient gave his written consent. Patients will be randomized to one of two arms: (1) Hypnosis or (2) Standard Of Care (SOC) A heart rate monitoring belt will be fitted to the patient for both groups. The patient will be asked to complete a self-assessment questionnaire on pain and stress, as well as socio-demographic parameters. A blood sample will be collected and the heart rate and blood pressure will be measured. Stitches will be taken with or without hypnosis, and after 30 minutes, the pain and stress self-assessment questionnaire will again be completed by the patient, and a new blood test will be taken. the heart rate monitoring belt will be removed, and the study will be completed for the patient.

Interventions

OTHERHypnosis

Before the beginning of stitches, the patient will be offered a hypnotic induction. The hypnotic induction is the initial phase of the hypnosis process. Its goal is to bring the patient to a state of dissociation: the hypnotic trance. Induction is usually achieved through progressive relaxation, sensory focusing, and a process of confusion.

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years old * Admitted in the emergency department of Clermont-Ferrand University Hospital * Stitchable wound * Patient's agreement

Exclusion criteria

* Pregnancy * Breast feeding * Refusal to participate * Patient not able to participate * Patients under guardianship, curatorship, deprived of liberty or safeguard of justice. * History of cardiac rhythm disorders (atrial fibrillation, pacemaker) * Psychotic disorder * Age \< 18 years old * Surgery needed * Patients who don't speak French * Wound of the eyelids, nose, ears or mouth * Deaf patients * Patients without a social security coverage * Nitrous oxyde use * Substance abuse * Head trauma with GSC ≤ 14 * Patient with endocrine diseases on the cortisol axis

Design outcomes

Primary

MeasureTime frameDescription
Heart rate variabilityHour 0The heart rate variability will be measured using Bittium Faros

Secondary

MeasureTime frameDescription
Changes on visual analog scale of pain and stressHour 0; Hour 0+30 minutesVisual analog scale (VAS) of pain and stress will be performed at two different times by the patient. A VAS is a 100-mm long horizontal line with verbal descriptors at each end to express the extremes of the feeling. Patients mark the point on the line that best corresponds to their pain and severity between 0 (no symptoms) to 100 (the worst pain and stress). Cut points on the pain VAS : no pain or low pain (0-29 mm), moderate pain (30-59 mm), and severe pain (\>59 mm). Cut points on the stress VAS : no pain or low stress (0-19 mm), moderate stress (19-49 mm), severe stress (50-81 mm), and at-risk stress (\>81 mm).
Evaluation of stress biomarkers in blood samplesHour 0; Hour 0+30 minutesEvaluation of cortisol, DHEA, DHEA-s, ghrelin, leptin, TNF-alpha, epinephrin, norepinephrine, dopamine
Evaluation of blood pressureHour 0; Hour 0+30 minutesEvaluation of hypnosis impact on systolic and diastolic blood pressure in millimeter of mercury (mmHg)
Evaluation of heart rateHour 0; Hour 0+30 minutesEvaluation of hypnosis impact on physiological parameters heart rate in beats per minute (bpm)
Impact of sociodemographics parameters on pain and stressHour 0; Hour 0+30 minutesEvaluation of the impact of sociodemographics parameters on pain and stress evaluated by the visual analog scale (VAS) performed at two different times (outcome N°2)
Impact of location of the wound on pain and stressHour 0; Hour 0+30 minutesEvaluation of the impact of location of the wound on stress and pain evaluated by the visual analog scale (outcome n°2)
Impact of location of the wound on variability of heart frequencyHour 0; Hour 0+30 minutesEvaluation of the impact of location of the wound on the variability of heart frequency measured by Bittium Faros (outcome n°1)
Impact of the length of the wound on pain and stressHour 0; Hour 0+30 minutesEvaluation of the impact of the length of the wound on stress and pain evaluated by the visual analog scale (outcome n°2)
Impact of the length of the wound on variability of heart frequencyHour 0; Hour 0+30 minutesEvaluation of the impact of the length of the wound on the variability of heart frequency measured by heart rate monitoring belt (outcome n°1)
Impact of the depth of the wound on pain and stressHour 0; Hour 0+30 minutesEvaluation of the impact of the depth of the wound on stress and pain evaluated by the visual analog scale (outcome n°2)

Countries

France

Contacts

CONTACTLISE LACLAUTRE
promo_interne_drci@chu-clermontferrand.fr+33473754963
PRINCIPAL_INVESTIGATORJean-Baptiste BOUILLON-MINOIS

University Hospital, Clermont-Ferrand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 11, 2026