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Preoperative Oral Heptaminol Hydrochloride in Preventing Hypotension After Spinal Anesthesia

Preoperative Oral Heptaminol Hydrochloride in Preventing Hypotension After Spinal Anesthesia in Lower Limb Surgeries With Tourniquet: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06564935
Enrollment
160
Registered
2024-08-21
Start date
2024-08-31
Completion date
2025-03-31
Last updated
2024-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypotension After Spinal Anesthesia

Brief summary

Methodologies and approaches have been implemented with differing degrees of success to prevent neuraxial hypotension. Currently utilized approaches to prevent hypotension during spinal anesthetic administration consist of physical precautions such as leg restraints and compression hosiery, as well as sympathomimetic medications Through a competitive inhibition of noradrenaline uptake, heptaminol hydrochloride prevented orthostatic hypotension and increased the plasma concentration of noradrenaline. This inhibitory effect might account for a portion of the antihypotensive effect After thorough research of the literature, studies evaluating the role of preoperative oral heptaminol hydrochloride in preventing hypotension after spinal anesthesia in lower limb surgeries with tourniquets are lacking.

Interventions

DRUGHeptaminol Hydrochloride

heptaminol hydrochloride will be administrated in its solution form 4ml/kg. The mean dose used will be 25 drops = 150 mg and will be given 1.5 to 2 hours before spinal anesthesia

DRUGPlacebo

Placebo drops (identical to heptaminol drops, prepared by the hospital pharmacy) will be administered 1.5 to 2 hours before spinal anesthesia.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Age from 18 to 50 years old. * Both sexes. * American Society of Anesthesiologists (ASA) physical status I-II. * Undergoing elective orthopedic lower limb operations with a tourniquet or plastic surgeries under spinal anesthesia.

Exclusion criteria

* Patient refusal. * History of hypertension, cardiovascular \[disorders of the heart and blood vessels and including coronary heart disease, rheumatic heart disease and other conditions\], and cerebrovascular diseases \[conditions that affect blood flow and the blood vessels in the brain. Problems with blood flow may occur from blood vessel narrowing (stenosis), clot formation (thrombosis), artery blockage (embolism), or blood vessel rupture (hemorrhage)\]. * Baseline SBP \>160 mm Hg before administration of the drug. * Any contraindications to spinal anesthesia such as coagulopathy, local skin infection, swelling, trauma, or deformity. * Medical conditions, which release vasoconstrictors such as pheochromocytoma. * Patients taking vasoconstrictors or uncorrected tachyarrhythmia. * History of drug allergy. * Psychiatric, neuromuscular disorder, major systemic diseases. * Pregnancy or lactating women. * Inadequate effect of spinal anesthesia or supplemented with other types of anesthesia.

Design outcomes

Primary

MeasureTime frameDescription
HypotensionIt will be assessed in the first 20 minutes after spinal anaesthesiaThe occurrence of hypotension is defined as SBP \<90 mm Hg or \<80% of baseline, after spinal anesthesia. Our hypotension outcome was a binary event (yes/no) defined as the occurrence of at least 1 episode for a patient below either threshold, versus none, across the repeated measurements.

Secondary

MeasureTime frameDescription
Changes in mean arterial blood pressure after spinal anesthesiaEvery 5 minutes in the first 20 minutes after spinal anesthesia then every 15 minutes until the end of operation assessed up to 3 hours after spinal anesthesiaDuration measurement of serial changes in mean arterial blood pressure after spinal anesthesia
Changes in heart rate after spinal anesthesiaEvery 5 minutes in the first 20 minutes after spinal anesthesia then every 15 minutes until the end of operation assessed up to 3 hours after spinal anesthesiaDuration measurement of serial changes in heart rate after spinal anesthesia

Other

MeasureTime frameDescription
Requirements of ephedrineFrom the time of intrathecal injection of the anesthetic drug until the end of operation after spinal anesthesia assessed up to 3 hours after spinal anesthesiaThe total requirements of ephedrine to treat hypotension
Requirements of AtropineFrom the time of intrathecal injection of the anesthetic drug until the end of operation after spinal anesthesia assessed up to 3 hours after spinal anesthesiaThe total requirements of ephedrine to treat bradycardia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026