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Virtual reality goggles ease colonoscopy pain, study finds

NCT ID NCT07496333

Symptom relief Sponsor: Max Healthcare Insititute Limited Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether using virtual reality (VR) during a colonoscopy can help patients feel less pain and anxiety, and reduce the need for sedative drugs. 84 adults aged 18 to 80 took part. The idea is that VR distracts the brain, making the procedure more comfortable and potentially safer by lowering medication side effects.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

84 people

The number who actually took part.

Started

Oct 2023

Finished

Oct 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. age 18 to 80 years; 2. absence of any history of overt or borderline psychiatric disorders; 3. abstinence from psychoactive medications. - Exclusion Criteria: 1. hearing and visual disorders; 2. psychiatric illnesses; 3. chronic pain disorders; 4. Alzheimer's disease or other dementia disorders; 5. a history of taking psychoactive drugs; 6. a history of taking beta blockers and Buscopan. 7. any contraindication including allergy to either midazolam or fentanyl. 8. those who opt for general anaesthesia. 9. Epilepsy 10. Balance disorders 11. Claustrophobia -

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Valid mesh conditions

Contacts and locations

Locations

  • Max Institute of Medical Education

    New Delhi, Saket, 110017, India

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