Open-Label Placebo for Acute Pain Relief

Boosting Open-Label Placebo Effects in Acute Induced Pain in Healthy Adults

Recruiting N/A Interventional Study
Acute Pain
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 65
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
141 (estimated)
Sponsor
University Hospital, Basel, Switzerland · Other
Who this trial is looking for

This trial is looking for healthy adults aged 18 to 65 years to study how an open-label placebo can help relieve acute pain. Participants will undergo a controlled pain simulation and receive a placebo treatment while their pain response is evaluated.

Are You a Good Fit for This Trial?
Must not be taking AnalgesicsOpioidsAntihistaminesCalcium channel blockersPotassium channel blockersSerotonin/noradrenaline reuptake inhibitors

You may be able to join if

  • I am a healthy adult aged 18 to 65
  • I have a body mass index (BMI) between 18 and 25
  • I can understand the study and pain rating system
  • I can give my informed consent

You may not be able to join if

  • I have participated in a previous open-label placebo study
  • I regularly take medications that can affect pain sensation
  • I have neuropathy
  • I have chronic pain
  • I have a neuromuscular disease
  • I have a dermatological disease
  • I have a psychiatric disease
  • I am pregnant or breastfeeding

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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Check Your Eligibility
About This Trial
This study is to investigate the effect of open-label placebo (OLP) application on acute pain in an experimental model of acute pain (simulating wound pain: this installation will apply monophasic, rectangular electrical pulses of 0.5ms duration with alternating polarity at 2 Hz frequency. The current will be increased to target a pain rating of 6 of 10 on the NRS (0 = no pain, 10 = worst imaginab…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Healthy volunteers (ASA Class I or II), aged 18 to 65 years * BMI between 18 and 25kg/m2 * Able to understand the study and the NRS * Able to give informed consent Exclusion Criteria: * Participation in a previous open-label placebo study; for Part 2, this includes Part 1 of…
Contacts

Tobias Schneider, MD

+41 61 328 65 43

tobias.schneider@usb.ch

CONTACT