Rigshospitalet
Copenhagen, 2100, Denmark
NCT Number: NCT01213654
A pilot study to observe satisfaction of analgesia with intercostal catheters after VATS lobectomy.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Copenhagen, 2100, Denmark
Pain and satisfaction with pain treatment is investigated in a population after VATS lobectomy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Age of consent (ie age>=18) Eligible for lobectomy Able to comply Willing to register postoperatively
-
Exclusion criteria
Time frame: Until discharge (2-4 days)
Painscore
Time frame: until discharge, 2-4 days
qualitative measurement
Time frame: until discharge, 2-4 days
Daily presence of, Nausea Dizziness Vomiting Sedation Pruritus
Rigshospitalet, Denmark
Other
Pain Relief After VATS Lobectomy Using Interoperatively Placed Inter Costal Catheters.
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06746948
Lung Cancer Patients, Lung Cancers
Changsha, China
View Trial DetailsNCT07024433
Lung Cancer Patients, Lung Diseases
Fuzhou, Fujian, China
View Trial DetailsNCT06725225
Lung Cancer Patients, Lung Diseases
View Trial DetailsNCT07062393
Lung Cancer Patients
Taipei, Taiwan
View Trial Details