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NCT Number: NCT07033949

Effect of Green Light Exposure at Different Times on the Pain of Subjects

Patients who met the criteria and needed to undergo elective surgery via arterial and venous puncture were included in this center. They were randomly divided into three time periods (8:00-9:00, 12:00-13:00, 16:00-17:00) and were exposed to green light (experimental group) and transparent light (control group) respectively. The effects of green light exposure on acute perioperative pain in patients were observed at different times.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Second Affiliated Hospital of Chongqing Medical University

Chongqing, Chongqing Municipality, 4000000, China

About this study

Random numbers were generated by the computer to randomly assign patients who met the inclusion and exclusion criteria to the experimental group (exposed to green light) and the control group (exposed to transparent light). The patients were randomly assigned to three time periods (8:00-9:00, 12:00-13:00, 16:00-17:00) to receive a colored exposure with glasses: Therefore, in order to minimize bias and expectations, it was not informed to the patients which color would affect the pain during the arterial puncture. The patients rested in the pre-anesthesia room for 5 minutes, their heart rate (HR) was measured, and a pain sensitivity test (tender point) was conducted. Then, the patients wore the trial glasses and stayed in the pre-anesthesia room for 30 minutes, and they underwent arterial and venous punctures. While monitoring the patients' heart rate, the catheterization of the arterial and venous punctures was performed. Then, during the arterial and venous puncture, their pain scores (NRS) were recorded separately.

exposed to green light (green group) for 30 minutes. The above operation will be repeated to measure the patient's pain threshold.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age range: 18 - 50 years old.
  • ASA classification: I - III.
  • Planned to undergo abdominal surgeries requiring general anesthesia and arterial puncture (this is not necessary for the healthy volunteer group).
  • Obtained informed consent from the patients.

Exclusion criteria

  • Skin ulceration, allergic reactions, or dermatitis at the tested area.
  • Long-term use of analgesics or psychiatric medications.
  • History of color blindness or uncorrected cataracts.
  • Severe cardiovascular or respiratory diseases, inflammatory disorders, etc.
  • Failure of the first arterial puncture.
  • Communication difficulties, etc.

Treatment and study plan

Green light glasses

Device

Exposure to green light for 30 minutes

Transparent light exposure

Device

Exposure to transparent light for 30 minutes

Primary outcomes

  1. Pain intensity during arteriovenous puncture

    Time frame: The pain score during arterial puncture which about 2-3min

    assessed using number rating scale (0 to 10, which higher scores mean a worse pain intensity)

Secondary outcomes

  1. Pain sensitivity

    Time frame: from the time before to 30 min after light exposure

    assessed by pressure pain stimulation (magnitude of pressure, kilogram per square centimeter)

  2. Analgesic consumption during surgery

    Time frame: From surgery beginning to the ending of the surgery

    assessed by the actual dose of analgesic during the surgery

  3. Pain intensity after surgery

    Time frame: From ending of the surgery to 24 hours after surgery

    assessed using number rating scale (0 to 10, which higher scores mean a worse pain intensity)

  4. Analgesic consumption after surgery

    Time frame: From ending of the surgery to 24 hours after surgery

    assessed by the actual dose of analgesic after surgery

Other outcomes

  1. Heart rate

    Time frame: from before arterial puncture to 5min after the arterial puncture

    assessed by the monitor using beat per minute

Study contacts

Contact information is provided by the study sponsor or research team.

guangyou ph.D Duan

CONTACT

[email protected]

18323376014

Sponsors and collaborators

Lead sponsor

The Second Affiliated Hospital of Chongqing Medical University

Other

Registry information

Official study title

A Randomized Controlled Study on the Effect of Green Light Exposure at Different Times on the Pain of Subjects

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jun 24, 2025
Registry last updated
Jun 27, 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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