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Completed

NCT Number: NCT07013071

Hemodynamic Effects of Different Vasoconstrictors in Mandibular Exodontia

Title of Study:

The Effect of Different Vasoconstrictive Agents on Hemodynamics Among Patients Undergoing Simple Mandibular Exodontia: A Triple-Blind Randomized Controlled Trial

Location:

King Abdulaziz University Dental Hospital (KAUFD), Jeddah, Saudi Arabia What Is This Study About?

This study examines two types of vasoconstrictive agents used alongside local anesthetic during simple lower tooth extractions:

* Epinephrine (1:100,000) * Epinephrine Bitartrate (1:55,000)

What are vasoconstrictors? Vasoconstrictors help control bleeding and extend the numbing effect during dental procedures. They are usually added to local anesthetics (numbing agent) during dental procedures. This research aims to answer the following questions:

1. Which one of the vasoconstrictive agents has less effect on the heart rate and blood pressure 2. Which one offers better pain control?

Who Can participate?

* Adult patient +18 year/old or above (healthy or with well-controlled conditions like hypertension) * Patients who require non-surgical lower tooth extractions * Procedures will be done by supervised fifth and sixth-year dental students

Potential Risks and Discomforts

Like any medical procedure, there are some potential risks, including:

From the anesthesia and vasoconstrictors:

* Allergic reaction * Prolonged numbness * Changes in blood pressure and heart rate

From the tooth extraction itself:

* Bleeding * Pain or discomfort * Swelling or bruising * Infection * Dry socket * Delayed healing * Damage to nearby teeth or tissues * Fracture of the tooth or jawbone * Numbness or altered sensation (temporary or permanent) * Sinus complications (in upper tooth extractions) * The need for additional procedures

Potential Benefits

* Free tooth extraction * Blood pressure monitoring - with referral to a primary care provider if undiagnosed high blood pressure is detected

Costs There are no additional costs to participate in this research. Treatment and extraction are provided free of charge.

Compensation / Treatment for Injury

If a participant is injured as a result of being in this study:

* Necessary treatment and medical care will be provided by the research team. * No financial compensation is available from King Abdulaziz University Dental Hospital (KAUFD).

Confidentiality Participants' identity and medical information will be kept confidential. Only authorized researchers and relevant oversight bodies may access Participants' medical/dental records for monitoring or auditing purposes, in accordance with laws and regulations. Any published results will not identify the participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

King Abdulaziz University, Faculty of Dentistry

Jeddah, Mecca Region, Saudi Arabia

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18 years or older.
  • ASA I or II classification (i.e., healthy or with mild systemic disease).
  • Requiring simple mandibular tooth extraction, as defined by painless removal with minimal tissue trauma and smooth postoperative healing.
  • Willing and able to provide informed consent.
  • Able to comply with study procedures (able to undergo the simple tooth extraction).

Exclusion criteria

  • Pregnant or lactating individuals.
  • ASA III or higher classification (i.e., patients with severe systemic disease).
  • Patients with uncontrolled systemic disease.
  • History of malignancy.
  • Presence of unstable psychiatric illness.
  • Current use of antiplatelet or anticoagulant medications.
  • Known allergies to local anesthetics.
  • Uncooperative patients or those with intellectual disabilities.
  • Cases requiring surgical extractions (e.g., needing tooth sectioning, mucoperiosteal flaps, or bone removal).
  • Patients requiring maxillary tooth extraction.
  • Presence of fascial space infection or acute oral conditions.

Treatment and study plan

2% Mepivacaine with 1:100,000 epinephrine

Drug

A standard vasoconstrictor-containing local anesthetic used in dental procedures to minimize bleeding and prolong anesthetic effect.

2% Mepivacaine with 1:55,000 Epinephrine Bitartrate

Drug

An alternative formulation of vasoconstrictor-containing local anesthetic evaluated for its safety and analgesic effectiveness in dental extractions.

Primary outcomes

  1. Change in Systolic and Diastolic Blood Pressure

    Time frame: Measured preoperatively, 3 minutes post-anesthesia (intraoperative), and immediately after the procedure (postoperative).

    To compare changes in systolic and diastolic blood pressure between the two groups (epinephrine vs. epinephrine bitartrate) at three time points: before administration of local anesthesia, 3 minutes after administration (intraoperative), and postoperatively following simple mandibular tooth extraction.

  2. Change in Heart Rate

    Time frame: Measured preoperatively, 3 minutes post-anesthesia (intraoperative), and immediately after the procedure (postoperative).

    To evaluate changes in heart rate between the two intervention groups across the same three time points to assess the hemodynamic impact of the vasoconstrictors used.

Secondary outcomes

  1. Pain Score Using Visual Analogue Scale (VAS)

    Time frame: Assessed every 30 minutes during the procedure and once at the completion of the extraction.

    To compare pain perception during and after the dental procedure between the two groups using a 10-point Visual Analogue Scale (VAS). Patients reported pain at 30-minute intervals throughout the procedure and at the end of treatment. The minimum value on the VAS is 0 and the maximum is 10.

Sponsors and collaborators

Lead sponsor

King Abdulaziz University

Other

Registry information

Official study title

The Effect of Different Vasoconstrictive Agents on Hemodynamics Among Patients Undergoing Simple Mandibular Exodontia: A Triple-Blind Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jun 10, 2025
Registry last updated
Jun 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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