Phase 3 Peripheral Neuropathy Trial, Recruiting NCT05624138 Sponsor: Tanta University Condition: Peripheral Neuropathy
Back to Peripheral Neuropathy

Phase 3 Peripheral Neuropathy Trial, Recruiting

NCT05624138
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been confirmed through a tissue test (biopsy) to have Stage III colorectal cancer (cancer of the colon or rectum).
  • People who are planned to receive a specific chemotherapy regimen called modified FOLFOX-6.
  • People who have no medical reasons preventing them from receiving chemotherapy.
  • People aged 18 years or older, of any gender.
  • People whose blood test results show healthy enough levels of white blood cells, platelets, and red blood cells (confirm specific numbers with trial site).
  • People whose kidneys are working well enough, based on blood and/or urine tests (confirm specific values with trial site).
  • People whose liver is working well enough, based on a blood test measuring bilirubin levels (confirm specific values with trial site).
  • People who are generally well and able to carry out daily activities, rated 0 or 1 on a standard cancer health scale called the ECOG score (meaning fully active or able to do light activity).

Who may not be able to join:

  • People under 18 years of age.
  • People who have received certain nerve-damaging chemotherapy drugs (such as oxaliplatin, cisplatin, vincristine, paclitaxel, or docetaxel) within the 6 months before the trial.
  • People who already have nerve damage (peripheral neuropathy) caused by another condition, such as diabetes, a brain tumour, or a brain injury.
  • People with diabetes or other conditions known to increase the risk of nerve damage, such as an underactive thyroid, autoimmune diseases, or hepatitis C.
  • People with a known allergy to oxaliplatin or similar platinum-based chemotherapy drugs.
  • People with other inflammatory or physically stressful medical conditions (confirm with trial site).
  • People with glaucoma, cataracts, other long-term eye conditions, seizures, diabetes, heart disease, low blood pressure, dizziness, vertigo, Ménière's disease, or other disorders of the brain or nervous system.
  • People currently taking multivitamins containing vitamins E, C, or A; tricyclic antidepressants; or certain nerve-related medications such as gabapentin, lamotrigine, carbamazepine, or phenytoin.
  • People currently taking the medications amifampridine, bupropion, or donepezil.
  • People who have another active cancer that started in a part of the body other than the colon or rectum.
  • People who are pregnant or breastfeeding.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 13 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 00201111103067

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Tanta University
Registry
ClinicalTrials.gov
Start date
9 November 2022
Est. completion
4 April 2024

Where this trial is recruiting

🇪🇬 Egypt

Primary endpoints

variation in 12-item neurotoxicity questionnaire (Ntx-12) total score; variation in pain rating scale score; the percentage of patients with peripheral sensory neuropathy grade ≥ 2

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov