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Experimental donor-cell treatment delivered through surgery

This study investigates cells grown from a donor and delivered using brain surgery in people with Parkinson's.

Testing a treatment or activity · Study reference: CTRI-2010-091-000432

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.

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Looking for volunteers

Start (reported date)
2010-01-08

Planned dates can move. A study finishing does not tell us when a paper will be published.

No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Age range not listed · Ask the team who can join

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Read all the rules for taking part

Sex eligibility reported by registry: Not reported

Inclusion criteria: Inclusion of patients for therapy will be under the investigator's discretion. However the following criteria will be considered. 1. Should be in the age group of 18-80 years. 2. Should be fully conscious, alert and oriented while providing consent 3. Should show significant motor and non motor symptoms 4. Subject should understand the requirements of study 5. Subject should provide a written informed consent and agree to return for Follow up 6. Subject should be clinically diagnosed for Parkinson's disease with motor complications despite adequate oral anti-parkisonian therapy. 7. Should be able to comply with and understand the required visit schedule and complete the same. Exclusion criteria: Exclusion of patients from therapy will be under the investigator's discretion. However the following criteria will be considered 1. Patient is suffering from Dementia (MMSE <25) 2. Patient is suffering from a neurodegenerative disorder other than Parkinson. 3. The extent or severity of the disease is not measurable. 4. If the subject suffers from pre-existing medical conditions such as bleeding disorders, septicemia. 5. Patients with a past (within one year) or present history of psychiatric disorder. 6. If the subject has been enrolled in other investigational drug trial or has completed any trial within the last 3 months. 7. If Hemoglobin < 10gm/dl, Serum Creatinine< 2mg/dl serum total bilirubin< 2mg /dl and HbA1c<7? 8. Pregnant or nursing or women in child bearing age without adequate contraception. 9. The subject tested positive for HIV, HCV, HBV,or VDRL
Full study name & original research details

Official study title

Clinical study on the use of ex vivo expanded allogeneic mesenchymal stem cells for Parkinson's disease

Original description

Intervention: Intervention1: single injection using precoronal burr hole surgery: 4 million cells/kg body weight. Control Intervention1: NIL: NIL Primary outcome: Primary Outcome measures: 1At 1, 3, 6 and 12 months after discharge, patients will have follow-up examinations to assess their clinical status and to review their current medication. 2Clinical improvement will be defined as a decrease in the specific symptom and lesions. 3UPDRS will be repeated in all patients. Apart from the routine Proforma for Parkinsonism, the UPDRS will be done at the baseline and at the 12th month. 4Safety and tolerability, assessed by adverse events 5Quality of life Timepoint: 3,6,9,12 months Secondary outcome: Secondary Outcome will be the change in the baseline in UPDRS. Timepoint: 3,6,9,12 months

Conditions reported: Not reported

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Interventional
Interventions
Intervention1: single injection using precoronal burr hole surgery: 4 million cells/kg body weight. Control Intervention1: NIL: NIL
Phases
N/A
Sponsor
ADVANCED NEURO-SCIENCE ALLIES PVT. LTD#560, Bhargavi, 9th "A" Main, Indiranagar, Bangalore-560 038Karnataka (INDIA)
Start date reported by registry
2010-01-08 (reported)

Registry updated: Not reported · Status last verified by the registry submitter: Not reported

Registry records retrieved 2026-10-14 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Mrs. Vijaylakshmi A · +91-080-43312222 · satishtotey@ansaresearch.com

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

Facility not reported

India

Status not reported

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.