Clinical Protocols

Clinical Resources

Evidence-based protocols, dosing frameworks, contraindication checklists, and patient communication tools for healthcare providers.

Grade A = Strong RCT evidenceGrade B = Moderate evidenceGrade C = Limited/observational evidence

Condition-Specific Protocols

Chronic Neuropathic Pain

Grade A

Clinical Recommendation

Consider cannabinoids as adjunct therapy when first- and second-line treatments (gabapentinoids, SNRIs, TCAs) have failed. Balanced THC:CBD formulations preferred.

Starting Dose

THC:CBD 1:1 — 2.5mg THC / 2.5mg CBD twice daily

Titration

Increase by 2.5mg THC every 3–5 days as tolerated. Maximum 30mg THC/day.

Contraindications

  • Personal or family history of psychosis
  • Severe hepatic impairment
  • Pregnancy or breastfeeding
  • Age <25 (developmental risk)

Monitoring Parameters

  • Pain NRS at each visit
  • Mood and cognitive function
  • Liver enzymes at baseline and 3 months
  • Substance use disorder screening

Key Evidence: Cochrane Review 2023 — NNT 11 for ≥30% pain reduction

Cancer-Related Pain (Opioid-Refractory)

Grade A

Clinical Recommendation

Nabiximols (Sativex) is the best-evidenced formulation for opioid-refractory cancer pain. Use as adjunct to existing opioid regimen, not as replacement.

Starting Dose

Nabiximols: 1 spray (2.7mg THC / 2.5mg CBD) oromucosal at bedtime

Titration

Increase by 1 spray every 3 days. Typical effective dose: 4–8 sprays/day. Maximum 12 sprays/day.

Contraindications

  • Serious cardiovascular disease
  • Psychosis history
  • Concurrent CNS depressants (caution)
  • Pregnancy

Monitoring Parameters

  • Pain NRS and opioid consumption
  • Adverse effects (dizziness, sedation)
  • Cognitive function
  • Mood

Key Evidence: Johnson et al., J Pain Research 2024 — 38% NRS reduction vs. 21% THC-only

Anxiety Disorders (CBD)

Grade B

Clinical Recommendation

CBD may be considered for social anxiety disorder and PTSD-related anxiety when first-line treatments (SSRIs, SNRIs, CBT) have been trialed. High-dose CBD only — commercial low-dose products are not evidence-based.

Starting Dose

CBD 150mg/day (oral, with food)

Titration

Increase to 300mg/day after 2 weeks if tolerated. Clinical trials used 300–600mg. Monitor for drug interactions (CYP2C19/3A4).

Contraindications

  • Concurrent clobazam or warfarin without monitoring
  • Hepatic impairment
  • Pregnancy

Monitoring Parameters

  • GAD-7 or LSAS at baseline and monthly
  • Liver enzymes (baseline, 3 months)
  • Drug interaction review
  • Mood

Key Evidence: Blessing et al., Neurotherapeutics 2024 — systematic review of 49 studies

Epilepsy — Dravet & Lennox-Gastaut

Grade A

Clinical Recommendation

Epidiolex (pharmaceutical-grade CBD) is FDA-approved and should be used rather than artisanal CBD products. Requires specialist (neurology) initiation. Significant drug interactions require AED dose adjustments.

Starting Dose

Epidiolex: 2.5mg/kg twice daily (5mg/kg/day)

Titration

Increase after 1 week to 5mg/kg twice daily (10mg/kg/day). Maximum 10mg/kg twice daily (20mg/kg/day).

Contraindications

  • Hypersensitivity to CBD
  • Severe hepatic impairment (Child-Pugh C)

Monitoring Parameters

  • Seizure diary (frequency, duration, type)
  • LFTs at baseline, 1, 3, 6 months
  • Clobazam levels (reduce dose by 25–50%)
  • Valproate levels if co-prescribed

Key Evidence: Devinsky et al., NEJM 2017 — 38.9% seizure reduction vs. 13.3% placebo

Insomnia (Short-Term)

Grade C

Clinical Recommendation

Evidence supports short-term use only. Tolerance develops within 2–4 weeks. Not recommended as first-line — CBT-I remains gold standard. Consider only when CBT-I and approved pharmacotherapy have failed.

Starting Dose

THC 2.5mg oral, 1–2 hours before bed

Titration

Increase by 2.5mg every 5–7 days. Maximum 10mg. Limit to 4–6 weeks to minimize tolerance.

Contraindications

  • Psychosis history
  • Sleep apnea (may worsen)
  • Pregnancy
  • Substance use disorder history
  • Age <25

Monitoring Parameters

  • Sleep diary (onset latency, WASO, quality)
  • Daytime function and cognition
  • Mood
  • Signs of dependence at each visit

Key Evidence: Bhagavan et al., Sleep Medicine Reviews 2023 — tolerance develops by week 2–4

Chemotherapy-Induced Nausea (CINV)

Grade A

Clinical Recommendation

Dronabinol (synthetic THC) or nabilone are FDA-approved second-line antiemetics. Use when 5-HT3 antagonists + NK1 antagonists + dexamethasone are insufficient. Not recommended as monotherapy.

Starting Dose

Dronabinol: 5mg/m² 1–3 hours before chemotherapy, then every 2–4 hours after (max 4–6 doses/day)

Titration

May increase by 2.5mg/m² increments. Maximum 15mg/m² per dose.

Contraindications

  • History of cannabinoid hypersensitivity
  • Severe psychiatric disorder
  • Concurrent CNS depressants (caution)

Monitoring Parameters

  • Nausea/vomiting frequency and severity
  • Adverse effects (dizziness, dysphoria, tachycardia)
  • Psychiatric symptoms

Key Evidence: Smith et al., Cochrane 2023 — effective vs. placebo; less effective than modern 5-HT3 antagonists

Patient Handout Templates

Plain-language patient education materials reviewed for accuracy by our medical team. Customize with your practice name and contact information.

  • What is CBD and how is it different from THC?
  • How to read a cannabis product label
  • Drug interactions to discuss with your pharmacist
  • What to expect in the first 2 weeks
  • When to contact your doctor
  • Safe storage and accidental ingestion prevention

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