Oocyte Retrieval Clinical Trial
— HypnoPOOfficial title:
Interest of Hypnosis in Virtual Reality on Nociception During Oocyte Retrieval in a Medically Assisted Reproduction Procedure: a Randomised Controlled Study
Verified date | December 2023 |
Source | Clinique Mutualiste la Sagesse |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Study on the effect of the virtual hypnosis mask in addition to local anaesthesia on anxiety and perioperative pain during oocyte puncture
Status | Completed |
Enrollment | 182 |
Est. completion date | May 26, 2023 |
Est. primary completion date | May 26, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: - Patient having an oocyte puncture as part of a medically assisted procreation procedure - Surgical procedure planned in the operating theatre under local anaesthesia at the Clinique Mutualiste La Sagesse - Patient capable of receiving and understanding information about the study and giving written informed consent. - Affiliated to a social security system Exclusion Criteria: - Patient's refusal to participate in a study - Patient having an oocyte retrieval as part of an oocyte donation - Unbalanced epilepsy. - Hearing and/or visual impairments that contraindicate the use of the virtual reality headset. - Patient with a poor understanding of the French language. - Medical indication to carry out the oocyte puncture under general anaesthesia - Drug allergy or hypersensitivity to PARACETAMOL - IBUPROFEN or NEFOPAM prescribed during the pre-medication. - Patient under legal protection |
Country | Name | City | State |
---|---|---|---|
France | Clinique mutualiste La Sagesse | Rennes | Bretagne |
Lead Sponsor | Collaborator |
---|---|
Clinique Mutualiste la Sagesse |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Analgesia Nociception Index (ANI) measurement | The level of pain perceived by the patient during the performance of a painful care procedure will be measured by the ANI index which reflects heart rate variability | during oocyte puncture procedure | |
Secondary | Anxiety with beck anxiety inventory | Measurement of anxiety by the Beck Anxiety Inventory, on admission to hospital and on return to the ward, 1 hour after the oocyte puncture | 1 hour before intervention and immediately after the intervention | |
Secondary | Simulator Sickness Questionnaire (SSQ) | Assessment of tolerance of virtual reality with SSQ ; SSQ is a scale of cyber sickness from 0 to 48, a higher score mean a worse outcome. | Immediately after the intervention | |
Secondary | Analog visual scale (AVS) | Pain evaluation with Analog visual scale by the patient himself from 0 to 10, a higher score mean a worse outcome. | Immediately after the intervention | |
Secondary | Post intervention analgesic therapy | Identify the need for postoperative analgesic treatment in the two groups | Immediately after the intervention | |
Secondary | Total duration of the procedure of oocyte ponction (min) | Total duration of the procedure (min), from the beginning of local anesthesia to the end of the oocyte retrieval | From the first ponction of local anesthesia to the end of the retrieval of the last oocyte | |
Secondary | Conversion rate from local anaesthesia to unplanned general anaesthesia | Conversion rate in percent | Immediately after the intervention | |
Secondary | Gynecologist's numerical satisfaction scale | Measure by a numerical scale out of 10, a higher score mean a better outcome. | Immediately after the intervention | |
Secondary | Patient's numerical satisfaction scale | Measure by a numerical scale out of 10, a higher score mean a better outcome. | Immediately after the intervention |
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