Convolvulus pluricaulis for Health & Longevity - Quick Reference Sheet

Convolvulus pluricaulis for Health & Longevity

Created on 08/25/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5 Audit

An inexpensive Indian herb used for memory and calm for two thousand years, with research broad in animals and thin in people. Nothing has been tested against a placebo. Young adults reported better delayed recall after two months. Combining it with the anti-seizure drug phenytoin is the one documented harm; verified identity and metal testing outrank dose refinement. (Full Review)

Protocol

Whole-powder course (traditional Ayurvedic approach)
3-6 g twice daily
Dried whole-plant powder with warm water or milk after food. 6 g twice daily for 45 days is the highest verified human dose.
Processed-tablet course
500 mg twice daily
Tablets after food with milk, for two months. Both human cognitive studies used juice-processed tablets.
Best time of day
Evening or morning
Evening for calming and sleep use, morning for cognitive use. Split, twice daily after food is the only validated condition.
Time to effect
Memory and delayed recall
45-60 days
Memory changes were measured only at 45-60 days in every human study, so a fair evaluation window is two months, not two weeks.
Menopause symptom and anxiety burden
45 days
Favourable direction across all four scales after 45 days at 6 g twice daily.
Sedation and calm
Within hours
Sedative and calming effects appear within hours of the first doses.

Benefits

Contraindications
  • Anyone taking phenytoin, or with epilepsy of any type not stably controlled for 12 months
  • Pregnancy and lactation, at any dose
  • Symptomatic hypotension, or seated systolic blood pressure below 100 mmHg
  • Untreated or under-replaced hypothyroidism (thyroid-stimulating hormone above 4.0 mIU/L)
  • Scheduled surgery or general anaesthesia within 14 days
  • Children and adolescents under 16
Key Interactions
  • Other anti-seizure medications (caution): carbamazepine, valproate, lamotrigine, levetiracetam
  • Antihypertensive drugs (caution): lisinopril, losartan, amlodipine, indapamide
  • Sedatives and central depressants (caution): benzodiazepines (diazepam), Z-drugs (zolpidem), opioids (oxycodone), alcohol
  • Levothyroxine and thyroid replacement (monitor)
  • Glucose-lowering drugs (monitor): metformin, sulfonylureas (glipizide), insulin
  • Over-the-counter medications (caution): sedating antihistamines (diphenhydramine), dextromethorphan
  • Supplement interactions (caution): valerian, kava, magnesium glycinate, melatonin, L-Theanine, huperzine A, Bacopa monnieri, alpha-GPC
  • Supplements with additive blood-pressure lowering (caution): Rauvolfia serpentina, beetroot nitrate, hibiscus, aged garlic extract, high-dose omega-3
  • Other interventions (caution): anaesthesia, elective surgery, electroconvulsive therapy, ketogenic or extended-fasting protocols

Risk & Side Effects

  • High:
  • Medium: Loss of seizure control when combined with phenytoin; heavy-metal contamination of Ayurvedic preparations; botanical substitution and misidentification
  • Low: Additive blood-pressure lowering
  • Speculative: Sedation and psychomotor slowing; suppression of active thyroid hormone; additive blood-glucose lowering

Monitoring

Marker Target Why
Seated blood pressure 110-125 / 70-80 mmHg The herb lowers blood pressure; detects additive drops
Thyroid-stimulating hormone 0.5-2.0 mIU/L Screens for the thyroid suppression seen in animals
Free T3 3.2-4.2 pg/mL The specific hormone reduced in the animal study
Fasting glucose 75-86 mg/dL Guards against additive lowering with diabetes drugs
LDL cholesterol Below 100 mg/dL, or below 70 mg/dL with added cardiovascular risk Tracks the animal lipid-lowering signal in humans
ALT 10-26 U/L in women, 10-33 U/L in men Herbal products can cause unpredictable liver injury
Whole-blood lead Below 1.0 µg/dL One-fifth of Ayurvedic products carry detectable lead
Plasma phenytoin 10-20 µg/mL total, only where phenytoin cannot be stopped Co-use lowered levels and broke through seizure control
Delayed-recall test score No established target; the change from the individual's own baseline is what is tracked The endpoint that both human studies actually moved

Cadence: Baseline fasting panel plus seated and standing blood pressure on two separate days; blood pressure twice weekly for the first four weeks, then monthly; thyroid function and glucose at 8-12 weeks; lipids and liver enzymes at 12 weeks; then every 6-12 months for as long as use continues.

Qualitative Assessment

  • Sleep latency and whether sleep feels deeper or merely longer
  • Morning alertness, and any next-day grogginess after evening dosing
  • Subjective calm under load, distinguished from flatness or indifference
  • Recall of names, lists and where objects were placed
  • Steadiness on standing quickly, and any lightheadedness
  • Coordination and reaction quality in skill-dependent training