Caralluma fimbriata for Health & Longevity - Quick Reference Sheet

Caralluma fimbriata for Health & Longevity

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

A wild Indian succulent sold as a capsule extract to curb hunger. Combining all trials leaves one small effect: reduced waist measurement and waist-to-hip ratio. Weight, blood sugar, and blood fats do not move, and the hunger claim is split. Well tolerated: mild, short-lived digestive upset and occasional rash. Nothing beyond sixteen weeks; the evidence base is commercially interested. (Full Review)

Protocol

Standard protocol
500 mg twice daily
Standardised hydroethanolic extract with food, totalling 1 g daily — the dose used in every published randomised trial
Timing
Morning and evening with meals
No trial compared timings; evening dosing has not been linked to sleep disruption in any trial
Standardised extract approach
Hydroethanolic extract
The branded Slimaluma extract from Gencor Pacific is the form used in essentially all clinical trials
Time to effect
Waist and body composition
8–16 weeks
Waist and body-composition changes required 8 to 16 weeks in trials
Appetite
About 4 weeks
Appetite changes, where they occur, appeared by about four weeks
Anxiety and perceived stress
4–8 weeks
Greater improvement than placebo on the anxiety and perceived-stress questionnaires at both 4 and 8 weeks

Benefits

Contraindications
  • Pregnant or breastfeeding women
  • Children and adolescents outside a supervised Prader-Willi protocol
  • Adults with a current or past eating disorder
  • Adults with clinically significant liver or kidney impairment (estimated glomerular filtration rate below 45 mL/min/1.73 m², or Child-Pugh Class B or C liver disease)
  • Adults above 65 with sarcopenia or unintentional weight loss
  • Anyone with known Apocynaceae family plant allergy
Key Interactions
  • Anticoagulants and antiplatelet drugs (warfarin, heparin, dalteparin, enoxaparin)
  • Glucose-lowering drugs (insulin, sulfonylureas such as glipizide, metformin)
  • Serotonergic psychiatric medication (selective serotonin reuptake inhibitors such as sertraline, appetite drugs acting on serotonin receptors)
  • Prescription weight-loss agents (semaglutide, phentermine)
  • Over-the-counter agents (bulk-forming laxatives, psyllium, loperamide, bismuth subsalicylate)
  • Supplements with additive appetite or glucose effects (Gymnema sylvestre, Garcinia cambogia, glucomannan, berberine, chromium)
  • Other interventions (prolonged fasting, aggressive calorie restriction, high-volume endurance training)

Risk & Side Effects

  • High: Gastrointestinal disturbance
  • Medium: Cutaneous hypersensitivity reactions; product adulteration, species substitution, and mislabelling
  • Low: Unverified safety in pregnancy and lactation; absence of human safety data beyond sixteen weeks
  • Speculative: Serotonergic interaction with psychiatric medication; hypoglycaemia when combined with glucose-lowering therapy

Monitoring

Marker Target Why
Waist circumference < 94 cm (men), < 80 cm (women) The only outcome with pooled trial support
Waist-to-hip ratio < 0.90 (men), < 0.85 (women) Second pooled-significant outcome; tracks fat distribution
Body weight and body fat percentage 10–20% fat (men), 18–28% (women) Detects whether any loss is fat or lean mass
Fasting glucose 75–86 mg/dL Baseline safety check and additive-hypoglycaemia guard
HbA1c 4.8–5.3% Confirms no adverse glycaemic drift over a cycle
Fasting insulin 2–5 µIU/mL Detects insulin-resistance change alongside waist reduction
Leptin 4–6 ng/mL (men), 8–12 ng/mL (women) The one biomarker that differed between groups in the longest trial
Lipid panel (triglycerides, HDL, LDL) Triglycerides < 100 mg/dL; triglyceride-to-HDL ratio < 2.0 Human trials showed no lipid benefit; measured as a safety check
ALT and AST ALT 10–26 U/L; AST 10–26 U/L Human clearance route is uncharacterised; liver disease was a trial exclusion
Creatinine and estimated glomerular filtration rate eGFR > 90 mL/min/1.73 m² Kidney disease was a trial exclusion criterion
Blood pressure < 120/80 mmHg One trial reported within-group systolic changes; confirms no adverse shift
Salivary cortisol (morning) No established target for this use; track change from the individual's own baseline Only relevant if using the extract for the stress endpoint

Cadence: Baseline panel before starting; waist circumference and body weight every 2 weeks; full biochemical panel at 12 weeks and at the end of a 16-week cycle; daily fasting glucose for 2 weeks on glucose-lowering medication.

Qualitative Assessment

  • Hunger between meals — rated 1 to 10 at a fixed time daily
  • Time to satiety within a meal, and portion size left uneaten
  • Frequency and intensity of food cravings, particularly evening cravings
  • Digestive comfort — stool frequency and consistency, bloating, nausea
  • Perceived stress and anxiety, if that is the reason for use
  • Sleep quality and time to fall asleep, given evening dosing and absent trial data
  • Training capacity and recovery, as a proxy for adequate fuelling