Patient-reported Pain and Symptom Relief During Three Months After Surgery for Benign Prostatic Hyperplasia

Recruiting Observational Study
Benign Prostatic Hyperplasia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
50 and older
Sex
Male
Study type
Observational
Participants needed
500 (estimated)
Sponsor
Sahlgrenska University Hospital · Other
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About This Trial
This is a prospective observational study in patients undergoing surgery for benign prostatic hyperplasia (BPH). The purpose of the study is to investigate in great detail patients' recovery after surgery for BPH regarding pain, hematuria, urine leakage and use of pain-relieving medications for three months postoperatively. Patient-reported outcomes after three different surgical methods will be …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients undergoing transurethral surgery for benign prostatic hyperplasia * Singed informed consent to participate Exclusion Criteria: * Non-swedish speaking patients
Contacts

Joakim BE Strömberg, MD, PhD

46-768-341-327

joakim.stromberg@vgregion.se

CONTACT