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HemodynamicsNCT07901023

Comparison of Mean Arterial Pressure After Endotracheal Intubation in Patients Undergoing Spine Surgery With Pre-emptive Nitroglycerine Versus Dexmedetomidine

A study testing Nitroglycerin (NTG) and Dexmedetomidine in people with Hemodynamics and Arterial Pressure, run by Mayo Hospital Lahore at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This randomized controlled study compared nitroglycerine and dexmedetomidine for controlling blood pressure after insertion of a breathing tube in adults undergoing spine surgery under general anesthesia. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Hemodynamics, Arterial Pressure
What is being tested?
Nitroglycerin (NTG) and Dexmedetomidine
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 sitePakistan
Study dates
10 Jan 2026to 10 Jun 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Patients aged 18-60 years.
  • Patients of either sex.
  • Patients undergoing elective discectomy, laminectomy, or other spine surgery under general anesthesia.
  • American Society of Anesthesiologists physical status class I or II.

Who cannot join

  • Known or suspected allergy to dexmedetomidine.
  • Patients with hypertension, diabetes mellitus, or cardiovascular disease.
  • Patients with peripheral vascular disease.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Mayo Hospital, Lahore

    Lahore, Punjab Province, 54000

Other trials in Pakistan

About this study

This randomized controlled study compared nitroglycerine and dexmedetomidine for controlling blood pressure after insertion of a breathing tube in adults undergoing spine surgery under general anesthesia. The study hypothesis was that average blood pressure, measured as mean arterial pressure, differed between patients who received the two medicines.

The study included 80 patients aged 18-60 years at the Department of Anesthesia, King Edward Medical University and its affiliated hospital in Lahore, Pakistan. Patients were randomly assigned by a lottery method to two groups of 40. One group received nitroglycerine through an intravenous infusion, while the other received dexmedetomidine. Both groups received the same general anesthesia protocol. Blood pressure was recorded before anesthesia and five minutes after insertion of the breathing tube. The main outcome was mean arterial pressure at five minutes after tube insertion, which was compared between the two groups.

Being tested
Nitroglycerin (NTG), Dexmedetomidine
Keywords
Nitroglycerin, Dexmedetomidine, Mean arterial pressure, Intubation, Intratracheal, Spine surgery

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nitroglycerin (NTG)Drug

    Nitroglycerin was administered by intravenous infusion at 120 micrograms/kg/hour and titrated to the target mean arterial pressure.

  • DexmedetomidineDrug

    Dexmedetomidine was administered intravenously, followed by a continuous infusion at 1.0 microgram/kg/hour, titrated to the target mean arterial pressure.

Study groups in NCT07901023
Study groupRoleWhat they receive
Group A: NitroglycerinActive comparatorForty participants received intravenous nitroglycerin during general anesthesia for elective spine surgery. The infusion was titrated to maintain mean arterial pressure between 60 and 70 mmHg.
Receives: Drug: Nitroglycerin (NTG)
Group B: DexmedetomidineExperimentalForty participants received intravenous dexmedetomidine during general anesthesia for elective spine surgery. The infusion was titrated to maintain mean arterial pressure between 60 and 70 mmHg.
Receives: Drug: Dexmedetomidine

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mean Arterial Pressure

    Mean arterial pressure was assessed using noninvasive blood pressure measurements and expressed in millimeters of mercury. It was calculated as [systolic blood pressure + (2 × diastolic blood pressure)] ÷ 3. Mean arterial pressure measured five minutes after endotracheal intubation was compared between the nitroglycerin and dexmedetomidine groups.

    Measured: Five minutes after endotracheal intubation.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Oct 2026
  2. Study start10 Jan 2026
  3. Primary completion10 Jun 2026
  4. Study completion10 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
80 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07901023
Sponsor's protocol ID
Mayo10
Status last verified
Oct 2026
First submitted
22 Oct 2026
Last updated
28 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Nitroglycerin (NTG) and Dexmedetomidine in people with Hemodynamics and Arterial Pressure, run by Mayo Hospital Lahore at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mean Arterial Pressure (time frame: Five minutes after endotracheal intubation.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2026.

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