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Patient Reported Experiences With Sparing External Oblique Fascia Vs Standard Inguinal Orchiectomy

Recruiting

Patient Reported Experiences With Sparing ExteRnal Oblique Fascia Vs Standard Inguinal OrchiEctomy

Who can join

Ages 18 and older · Men

Full eligibility criteria
Inclusion Criteria:

* Participants undergoing radical orchiectomy for suspected testicular malignancy
* Testicular malignancy can be germ cell tumor or non germ cell tumors, including paratesticular tumors as long as a radical orchiectomy is planned
* Participants over 18 years of age who can provide informed consent
* Participants not currently using opiates for another reason
* Regional and metastatic patients are allowed, as long as participant does not require opiates for pain related to metastatic disease
* No contraindication for participant to receive standardized medication pathway in the peri-operative period.

Exclusion Criteria:

* Clinical T4 disease
* History of illicit substance abuse (including prior opioid abuse) except for marijuana
* Participants who underwent chemotherapy or radiotherapy prior to orchiectomy
* Opioid use within 1 month of study enrollment
* Participants with large testis masses requiring skin incision larger than 8 cm in size.
* Participants with large testis masses requiring orchiectomy through an incision other than the standard transverse inguinal incision (i.e. hockey stick incision, vertical incision)

About the study

The purpose of this study is to evaluate the difference in patient-reported postoperative outcomes between two standard-of-care surgical techniques for radical orchiectomy (inguinal orchiectomy versus external oblique fascia sparing orchiectomy) for treatment of patients with suspected testicular malignancy. The main questions it aims to answer are:

1. Does sparing the external oblique fascia during orchiectomy reduce pain after surgery? 2. Is there a difference in narcotic consumption after surgery? 3. Is there a difference in neuropathic pain after surgery? 4. Is there a difference in complications after surgery?

What is being tested

Sponsor: Loma Linda University · Participants: 80 · Started: 2026-12

Contact the study team

Official record on ClinicalTrials.gov — NCT06828185

Locations in the U.S.

CaliforniaLoma Linda University, Loma Linda

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.