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

NCT ID: NCT06828185

Last Updated: 2026-02-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-05-31

Study Completion Date

2029-09-30

Brief Summary

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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?

Detailed Description

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Radical inguinal orchiectomy is the standard of care surgical approach for removing a testicle when clinically there is concern for testicular cancer. The procedure is generally minor and performed in the outpatient setting. Recent data demonstrates a trend towards high opioid prescription following this procedure in an attempt to minimize postoperative pain, which is associated with persistent new opioid use in the future. Numerous efforts have been put in place to minimize postoperative pain following scrotal procedures, with success noted when opioid sparing pathways have been adopted. However, there has been sparse data on modifications within surgical technique that could improve patient pain following this procedure.

There have been various descriptions of technique to performing a radical orchiectomy which involves removal of the diseased testicle and spermatic cord. Classically, performing a radical inguinal orchiectomy involves incision of the external oblique fascia to expose and ligate the spermatic cord. During this step, the ilioinguinal nerve is exposed and can be injured by either traction injury or inadvertent transection. Modifications to this technique have been described which involve sparing of the external oblique fascia. Both approaches are performed via a similar incision and both the testicle and spermatic cord are removed. In fascia sparing modification, the spermatic cord is controlled, dissected, and subsequently ligated at the level of the superficial inguinal ring without incising the external oblique fascia. Proponents of this approach suggest the potential for less convalescence and faster recovery due to less tissue manipulation and avoidance of disturbances to the ilioinguinal nerve. Despite this potential benefit, there is no evidence to demonstrate superiority of either approach as it relates to patient recovery.

Therefore, we propose a randomized single-blinded clinical trial investigating postoperative pain outcomes of inguinal radical orchiectomy compared to external oblique fascia sparing radical orchiectomy.

Conditions

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Testicular Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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Radical inguinal orchiectomy

Group Type ACTIVE_COMPARATOR

Radical inguinal orchiectomy

Intervention Type PROCEDURE

External oblique fascia will be incised during orchiectomy

Radical external oblique fascia sparing orchiectomy

Group Type ACTIVE_COMPARATOR

Radical external oblique fascia sparing orchiectomy

Intervention Type PROCEDURE

External oblique fascia will be spared during orchiectomy

Interventions

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Radical inguinal orchiectomy

External oblique fascia will be incised during orchiectomy

Intervention Type PROCEDURE

Radical external oblique fascia sparing orchiectomy

External oblique fascia will be spared during orchiectomy

Intervention Type PROCEDURE

Eligibility Criteria

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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)
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Loma Linda University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Loma Linda University

Loma Linda, California, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Muhannad Alsyouf, MD

Role: CONTACT

9095584000 ext. 44196

Brian Hu, MD

Role: CONTACT

9095584000 ext. 44196

Facility Contacts

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Muhannad Alsyouf, MD

Role: primary

909-558-4000 ext. 44196

References

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Shei A, Rice JB, Kirson NY, Bodnar K, Birnbaum HG, Holly P, Ben-Joseph R. Sources of prescription opioids among diagnosed opioid abusers. Curr Med Res Opin. 2015 Apr;31(4):779-84. doi: 10.1185/03007995.2015.1016607. Epub 2015 Feb 24.

Reference Type BACKGROUND
PMID: 25661018 (View on PubMed)

Other Identifiers

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5250002

Identifier Type: -

Identifier Source: org_study_id

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