Massive global study aims to ease Post-Surgery pain
NCT ID NCT02083835
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is a large international registry that collects information from patients after surgery to understand how well their pain is managed. Researchers will look at patient-reported outcomes like worst pain, side effects, and satisfaction with treatment. The goal is to improve pain care for future patients. Anyone 18 or older (or 4+ in a sub-study) who had surgery and is on the ward can join.
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.
- Participants
-
About 200,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jan 2009
- Expected to finish
-
Dec 2030
An estimate. End dates often move.
- 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.
Who is studied
adult post-surgical patients in hospitals on post-op day 1
- Ages
-
4 years and older
- 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 Hide 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: * \>= 18 years or \>= 4 years for sub-project QUIPSI/PAIN OUTinfant * patient is post-op day 1 * patient is at least 6 hours on the ward * patient has given consent Exclusion Criteria: * patient cannot communicate * patient is cognitively impaired * patient is asleep * patient is too ill * patient does not want to fill in the questionnaire
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Post operative pain are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Jena University Hospital
RECRUITINGJena, 07747, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Which nerve block wins the battle against chest surgery pain?
- Which nerve block wins the battle against Post-Surgery pain?
- Can a pre-surgery paracetamol and tramadol combo beat fentanyl for day-case pain?
- Insulin eye drops put to the test for faster corneal healing
- Can a Longer-Lasting nerve block cut opioid use after spine surgery?
- Could a simple mineral calm the Body's Post-Surgery fire?