Efficacy and Safety of Cyclophosphamide in the Treatment of Refractory Proliferative Arachnoiditis in Central Nervous System Tuberculosis- A Randomized Double Blinded Placebo Controlled Trial

Who is this study for? Patients with central nervous system tuberculosis
What treatments are being studied? Cyclophosphamide
Status: Unknown
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

Tubercular meningitis occurs in around 10% of those with extrapulmonary tuberculosis and is a major cause of mortality and morbidity. Inspite of effective Anti-tubercular drugs, still around 30% of patients develop complications due to arachnoiditis such as spinal tubercular radiculomyelitis, optico-chiasmatic arachnoiditis, development of new tuberculomas after starting therapy etc. which are probably immune mediated inflammatory responses due to paradoxical reaction to ATT. The management of arachnoiditis is far from satisfactory. High dose methylprednisolone, intrathecal hyaluronic acid, thalidomide have been tried in small case series and case reports. However, the results have not been satisfactory. There are two published reports of cyclophosphamide usage in TBM related vasculitis and stroke The investigators tried cyclophosphamide in four patients after consent, and found remarkable improvement in all of them. (Under peer review) In order to test this hypothesis, a randomized controlled trial is needed.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 14
Maximum Age: 60
Healthy Volunteers: f
View:

• Patients attending Neurology/Pulmonary Medicine/Medicine/Geriatric Medicine OPD/admitted in respective wards with proliferative tubercular arachnoiditis refractory to corticosteroids and standard Anti-tubercular drugs for CNS tuberculosis

• Atleast 14 years of age of all sexes

• Not more than 60 years of age at time of enrolment

• Patient was started on ATT for tubercular meningitis and had clearcut clinical improvement with resolution of fever/constitutional symptoms AND improvement in headache, vomiting and sensorium for atleast 10 days following which there is deterioration again due to arachnoiditis

• Developed paraparesis/quadriparesis/sphincter dysfunction due to spinal radiculomyelitis or vision loss due to due to optico-chiasmatic arachnoiditis with imaging evidence of arachnoiditis

• Has received standard ATT for atleast 3 months with adequate dose and compliance

• Received corticosteroids for treatment of arachnoiditis and deemed to be refractory to corticosteroids by the primary physician treating the patient

• MRI brain and spine are suggestive of Arachnoiditis

• CSF GeneXpert/Line Probe assay/cultures are not suggestive of drug resistant tuberculosis

• Reasonable clinical certainty OR allied investigations such as CECT chest/abdomen/PET CT ruling out drug resistant tuberculosis

• Other relevant investigations like CSF analysis not suggestive of alternative diagnosis such as cysticercal/ cryptococcal/other fungal infections/other causes of chronic meningitis such as brucella/ nocardia/ syphilis/recurrent viral meningitis/ carcinomatous/ lymphomatous meningitis or non infective causes such as sarcoidoisis/sub-arachnoid hemorrhage etc.

• Willing to undergo periodic assessment clinically and with MRI.

• Ready to provide consent for cyclophosphamide therapy

• Willing to adhere to protocol and comply with follow up visits

Contact Information
Primary
Arunmozhimaran Elavarasi, MD DM
arun_ela@yahoo.com
+919013844274
Backup
Padma Srivastava MV, MD DM
vasanthapadma123@gmail.com
+919868398261
Time Frame
Start Date: 2021-01-01
Completion Date: 2024-12-31
Participants
Target number of participants: 40
Treatments
Experimental: Cyclophosphamide arm
Participants randomized to the cyclophosphamide arm will be administered 750 mg/m2 body weight (rounded off to the nearest 50 mg above the calculated value) of cyclophosphamide diluted in normal saline every month (Total 6 months) along with equal dose of mesna 50% administered prior to infusion and 50% after the infusion of cyclophosphamide
Other: Placebo arm
Participants randomized to the placebo group will be given similar quantity of normal saline and mesna as described above
Sponsors
Leads: All India Institute of Medical Sciences

This content was sourced from clinicaltrials.gov