Recruiting NA Oral Melatonin

Compares treatment options for Oral Melatonin

Official title Effect of Oral Melatonin Versus Intraoperative Lidocaine Infusion on Incidence of Postoperative Delirium in Elderly Patients Undergoing Total Hip Arthroplasty

ClinicalTrials.gov ID: NCT06768580

What this study is testing

What is Melatonin?

Melatonin is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for oral melatonin.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
The aim of this study is to assess the effect of oral melatonin versus intraoperative lidocaine infusion on incidence of postoperative delirium in elderly patients undergoing total hip arthroplasty under spinal anesthesia.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 65 and older

You may be able to join if

  • Elderly patients aged \>65 years old undergoing unilateral total hip arthroplasty.
  • Patients with body mass index (BMI) (18-30) kg/m2.
  • American Society of Anesthesiologists (ASA) physical status I-III, scheduled to undergo unilateral total hip arthroplasty.

You likely can't join if

  • History of mental illness or scoring less than 8 using abbreviated mental test (AMT) before operation.
  • Obvious sinus bradycardia (heart rate of \<50 beats per minute) or other serious cardiovascular diseases.
  • Symptomatic cerebrovascular disease (such as previous stroke).
  • History of liver and kidney dysfunction.
  • Allergy to lidocaine or melatonin.
  • Metabolic disorders and fluid, electrolytes disturbances.
See the full eligibility criteria
Who can join
  • Elderly patients aged \>65 years old undergoing unilateral total hip arthroplasty.
  • Patients with body mass index (BMI) (18-30) kg/m2.
  • American Society of Anesthesiologists (ASA) physical status I-III, scheduled to undergo unilateral total hip arthroplasty.
What rules you out
  • History of mental illness or scoring less than 8 using abbreviated mental test (AMT) before operation.
  • Obvious sinus bradycardia (heart rate of \<50 beats per minute) or other serious cardiovascular diseases.
  • Symptomatic cerebrovascular disease (such as previous stroke).
  • History of liver and kidney dysfunction.
  • Allergy to lidocaine or melatonin.
  • Metabolic disorders and fluid, electrolytes disturbances.
  • Alcohol dependence or drug abuse.
  • Redo surgery or infectious complications.
  • CNS medications (antipsychotics, anticonvulsants, antiparkinsonian, antidepressants).
  • History of deep vein thrombosis.

The study team makes the final eligibility decision.

Where it's taking place

  • Tanta, El-Gharbia, Egypt

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 65 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Tanta, El-Gharbia, Egypt. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.