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Brain tumor study reveals hidden toll of chemo on daily life

NCT ID NCT03257618

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study followed 26 adults with low-grade glioma who were receiving chemotherapy (temozolomide) for the first time after surgery. Researchers measured how the treatment affected patients' quality of life, thinking skills, and emotional well-being over one year. The goal was to better understand the full impact of the disease and its treatment, since preserving quality of life is a key priority when a cure is not available.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

26 people

The number who actually took part.

Started

Jul 2017

Finished

Dec 2021

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adult patient aged ≥ 18, no age limit; * Histologically-proven DLGG; * Patient receiving TMZ as a first line treatment after surgery, whatever the delay between the surgery and the introduction of TMZ; * No previous oncologic treatment (except for surgery) for the DLGG; * Performance status (PS) score ≤ 2; * Absolute neutrophil count (ANC) ≥ 1500 cells/µL and platelet count ≥ 100 000 cells/µL; * Total serum bilirubin concentration ≤ 1.5 x the upper limit of normal (ULN); * Aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase ≤ 2.5 x the ULN; * Serum creatine concentration ≤ 1.5 x the ULN; * Negative pregnancy test in women of childbearing potential; * A signed informed consent obtained before any study specific procedures; * Patient fluent in French ; * Patient affiliated to a French social security system Exclusion Criteria: * Anaplastic glioma (WHO grade III glioma); * Impaired neurocognitive functioning defined by a score \< 22 at the MoCA evaluation; * Visual or auditory deficit ; * Previous chemotherapy for the DLGG; * Previous RT for the DLGG; * Known hypersensitivity to any of the study drugs, or excipients in the formulation; * Hypersensitivity to dacarbazine (DTIC); * Severe myelosuppression; * Problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption; * Legal incapacity or physical, psychological social or geographical status interfering with the patient's ability to sign the informed consent or to terminate the study; * Pregnant or breastfeeding women; * Men or women of childbearing potential who are unwilling to employ adequate contraception, from the beginning of the study until 6 months after administration of the last treatment dose; * Participation in another clinical trial with 30 prior to study entry.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Institut regional du Cancer - Val d Aurelle

    Montpellier, 34298, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.