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Clinical Trials/NCT07285356
NCT07285356RecruitingNot Applicable

GLOX-PEN: Phase II Clinical Trial to Evaluate the Use of Surgical Gloves for the Prevention of Oxaliplatin-Induced Peripheral Neuropathy

AC Camargo Cancer Center1 site in 1 country84 target enrollmentStarted: October 6, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
84
Locations
1
Primary Endpoint
Oxaliplatin-Induced Peripheral Neuropathy

Study Overview

Brief Summary

The primary objective of this randomized clinical trial is to assess whether the use of surgical gloves during treatment can prevent the occurrence of oxaliplatin-induced peripheral neuropathy.

Detailed Description

Gastrointestinal tumors account for one-quarter of the global cancer incidence and one-third of cancer-related deaths. Chemotherapy-induced peripheral neuropathy (CIPN) is a common adverse effect of oxaliplatin-based treatments. CIPN can lead to an extremely painful and debilitating process, causing significant loss of functional abilities and negatively affecting the quality of life of these patients, as well as activities of daily living (ADLs) such as walking, buttoning clothes, writing, brushing teeth, among others. This condition can even result in a state of vulnerability, with a high risk of falls and other injuries.

Primary Objective and Study Rationale:

Oxaliplatin, widely used to treat patients with colorectal neoplasms, is associated with chemotherapy-induced peripheral neuropathy (CIPN). Given the high prevalence and negative impact of CIPN on quality of life and adherence to cancer treatment, there is a significant gap in identifying effective prevention and management strategies. Although recent evidence suggests that surgical gloves (SG) can mitigate paclitaxel-induced peripheral neuropathy, SGs have not been tested for the prevention of oxaliplatin-induced peripheral neuropathy (OIPN). Therefore, the primary objective of this randomized clinical trial is to evaluate whether the use of SGs during treatment can prevent the occurrence of grade 2 or higher OIPN in the hands, as assessed by CTCAE v5.0 and PRO-CTCAE.

Secondary Objective:

To determine the relationship between Body Mass Index and the presence of sarcopenia, with the occurrence of OIPN; To evaluate the impact of OIPN on patients' health-related quality of life (HRQoL) using the EORTC QLQ-C30 questionnaire; To assess symptoms and functional limitations associated with OIPN using the EORTC QLQ-CIPN20 questionnaire.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients aged 18 years or older who have provided written informed consent.
  • Colon adenocarcinoma with high-risk stage III (pT4pN2) or stage IV.
  • Oxaliplatin-based treatment in the context of localized or metastatic disease.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

Exclusion Criteria

  • Pre-existing neuropathy.
  • Uncontrolled diabetes.
  • known glove allergies.
  • Prior treatment with paclitaxel, docetaxel or oxaliplatin.

Outcomes

Primary Outcomes

Oxaliplatin-Induced Peripheral Neuropathy

Time Frame: Baseline, 2 months, 4 months and 6 months

The primary objective of this randomized clinical trial is to evaluate whether the use of surgical gloves during treatment can prevent the occurrence of grade 2 or higher oxaliplatin-induced peripheral neuropathy in the hands, as assessed by CTCAE v5.0 .

Secondary Outcomes

  • Sarcopenia assessing by muscle strength, muscle quantity/quality, and physical performance, Body Mass Index (BMI) evaluated by a mathematical formula (kg/m2).(Baseline, 2 months, 4 months and 6 months)
  • Health-related Quality of life questionaries(Baseline, 2 months, 4 months and 6 months)
  • Functional limitations associated with OIPN(Baseline, 2 months, 4 months and 6 months)
  • Patient reported Peripheral Neuropathy(Baseline, 2 months, 4 months and 6 months)

Investigators

Sponsor
AC Camargo Cancer Center
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Virgilio Souza e Silva

Doctor and Head Oncologist of the Clinical Oncology Department at AC Camargo Cancer Center

AC Camargo Cancer Center

Study Sites (1)

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