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Comparison of 5 Buffering Agents on Changes in Salivary pH in Individuals Previously Exposed to a Test Fruit Juice (SALPH-F)

5 grudnia 2018 zaktualizowane przez: Dr Meru S

Comparison of Five Different Salivary Buffering Agents on the Changes in Salivary pH in a Cohort Previously Exposed to a Test Fruit Juice: A Randomized Controlled Crossover Trial.

The diurnal variation in the flow of saliva and hence the composition of saliva is an established fact. Consumption of most types of acidic and sweetened foods and beverages are known to reduce the pH of saliva and some of them even reduce it to critical pH levels and result in structural damage to the hard tissues of the tooth.

The purpose of this study is to ascertain the effect of the selected commercially available test fruit-juice drink on the salivary pH and assess the buffering capacity of the saliva with or without various intervention measures following the exposure to the test fruit-juice drink at different time intervals.

Przegląd badań

Szczegółowy opis

There are substantial existing evidences that there is diurnal variation in the flow of saliva and hence the composition of saliva. The average of normal pH of saliva is reported to be 6.8. Consumption of most types of acidic and sweetened foods and beverages are known to reduce the pH of saliva and some of them even reduce it to critical pH levels and result in structural damage to the hard tissues of the tooth.

Such damages can be prevented by maintaining the pH of saliva within optimal range by using oral hygiene measures.

The purpose of this study is to ascertain the effect of the selected commercially available test fruit-juice drink containing sugar on the pH of saliva and assess the buffering capacity of the saliva with or without various intervention measures following the exposure to the commercially available test fruit-juice drink at different time intervals.

Aims and Objectives:

  1. To measure the pH of saliva post-exposure to commercially available test fruit-juice drink after 5, 15, 30, 45 and 60 minutes.
  2. To measure the pH of saliva at 15, 30 and 45 minutes after using a tap water gargle as a buffering agent in those subjects who had prior exposure to commercially available test fruit-juice drink 15 minutes ago.
  3. To measure the pH of saliva at 15, 30 and 45 minutes after using a 0.2%Chlorhexidine mouth rinse as a buffering agent in those subjects who had prior exposure to commercially available test fruit-juice drink 15 minutes ago.
  4. To measure the pH of saliva at 15, 30 and 45 minutes after chewing Orbit® gum as a buffering agent in those subjects who had prior exposure to commercially available test fruit-juice drink 15 minutes ago
  5. To measure the pH of saliva at 15, 30 and 45 minutes after brushing with commercially available fluoridated tooth paste and soft brush as a buffering agent in those subjects who had prior exposure to test fruit-juice drink 15 minutes ago
  6. To measure the pH of saliva at 15, 30 and 45 minutes after gargling with 1% solution of baking soda as a buffering agent in those subjects who had prior exposure to commercially available test fruit-juice drink 15 minutes ago
  7. To compare the efficacy of buffering agents on the pH of saliva at 15, 30, 45 minutes post intervention in subjects who have had the commercially available test fruit-juice drink 15 min prior to the a specific intervention, with the pH of saliva recorded in the same subjects at the same time periods when no intervention with any buffering agent was carried out after having the commercially available test fruit-juice drink.
  8. To compare the pH of saliva recorded in the subjects at 15, 30, 45 minutes time periods when they used an intervention of gargle with tap water, with that recorded when they used mouth rinse of 0.2% Chlorhexidine, with that recorded when they brushed with soft brush and fluoridated tooth paste, with that recorded when they gargled with 1% baking soda solution and with that recorded when they chewed Orbit® chewing gum (15 minutes after using the test fruit-juice drink)

Materials and Methods:

30 volunteers in the age group of 18- 30 year with healthy oral cavities will be selected. Subjects with a history of any chronic medical illness, history of allergy, intake of drugs in the last 8 weeks, history of gastritis, bulimia will be excluded. Subjects with a DMFT score of more than 2 and Loe and Sillness Index of more than 0 will be excluded. Individuals who have and are currently undergoing orthodontic treatment will not be included in the study. Individuals who smoke or chew tobacco will not be included in the study sample. An informed consent for the research will be obtained from all the subjects who have volunteered for the study. The trial will be conducted as per the guidelines in the WHO-Handbook for Good Clinical Practice and the research protocol is approved by the Institutional Ethics Committee of the college.

The test fruit-juice drink that will be selected is Tropicana® Mixed Fruit Juice®.

The various buffering agents that will be used are:

  1. 0.2% Chlorhexidine mouth wash (Rexidine®, Indoco Remidies Ltd, Mumbai, India)- 10 ml solution swish for 60 sec and spit
  2. Tap water- 10ml swish for 60 sec and spit
  3. Brushing with fluoridated (Colgate Total®, Colgate-Palmolive Company, Mumbai, India) tooth paste- 2min using soft brush
  4. Chewing polyol containing gum (Orbit®, Wrigley Company)- chew for 5 minutes and spit
  5. Freshly prepared Sodium bicarbonate (baking soda) 1% w/v solution swish for 60 sec and spit.

The observer who will be measuring the salivary pH will remain blinded about the samples and buffering agent used.

The select individuals will be instructed to not use any mouth wash as part of oral hygiene regimen on test day and not consume any food or beverage for 2 hours prior to the collection of baseline sample of saliva at 10 AM on the test day. The select group of 30 individuals will be given a sample of 100 ml of Tropicana® mixed fruit-juice after recording their baseline salivary pH (0 min). They will be asked to sip, swish and swallow the drink within 2 minutes. After the exposure, salivary samples will be collected at 5 min and 15 min intervals for assessment of pH. Fifteen minutes after the exposure (consumption of test drink), the individuals will be asked to use one of the intervention methods included in this study. The salivary samples will be collected after 15, 30 and 45 minutes interval after the intervention. (i.e. 30, 45 and 60 minutes post exposure to the test drink respectively) The same protocol will be repeated using each intervention methods included in this study after a wash out period of minimum of 3 days. The protocol will be repeated on the study sample without any intervention following the exposure to the test fruit juice as a control.

Measurement of salivary pH will be done using a portable PH-035 Digital pH meter with automatic temperature compensation, to the accuracy of 0.1 and the machine will be calibrated on the morning of every test day and after 60 uses during the test day using Aquasol® pH calibration solutions with pH 4, 7 and 10.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

30

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Uttarakhand
      • Dehradun, Uttarakhand, Indie, 248140
        • Department of Oral Medicine & Radiology, Uttaranchal Dental & Medical Research Institute

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat do 30 lat (Dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • subjects in the age group of 18 to 30 years.
  • subjects with a DMFT index score of less than 2.
  • subjects with Loe and Silness index score of 0.
  • subjects willing to volunteer for the study.
  • subjects who are available for the whole study period of 4 months

Exclusion Criteria:

  • subjects with history of gastritis and bulimia.
  • subjects with chronic medical illness.
  • subjects with history of allergy.
  • subjects with history of drug intake for last 8 weeks.
  • subjects who smoke or chew tobacco.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Zapobieganie
  • Przydział: Randomizowane
  • Model interwencyjny: Zadanie krzyżowe
  • Maskowanie: Pojedynczy

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny komparator: Group 1: no intervention

The subject collects the unstimulated saliva in a sterile glass dish for the measurement of baseline pH of the saliva.The subject is then given 100 ml of test mixed fruit juice,Tropicana® Mixed Fruit Juice, (PepsiCo, Inc) to drink. The subject will sip, swish and swallow the drink within 2 minutes.

Unstimulated saliva samples are collected from the subject to measure the pH of saliva after 5, 15, 30, 45 and 60 minutes of consumption of the test mixed fruit juice.

Unstimulated saliva samples are collected from the subject to measure the pH of saliva after 5, 15, 30, 45 and 60 minutes of consumption of the test mixed fruit juice without any intervention.
Eksperymentalny: Group 2: tap water gargle

The subject collects the unstimulated saliva in a sterile glass dish for the measurement of baseline pH of the saliva.The subject is then given 100 ml of test mixed fruit juice,Tropicana® Mixed Fruit Juice, (PepsiCo, Inc) to drink. The subject will sip, swish and swallow the drink within 2 minutes.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva after 5 and 15 minutes of consumption of the test mixed fruit juice.

The subject will use 10 ml of tap water as mouth rinse to swish for 60 seconds and spit. Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva at 15, 30 and 45 minutes after the subject completes the gargle as an intervention.

Osoba badana użyje 10 ml wody z kranu do płukania jamy ustnej, aby przez 60 sekund chrząkać i pluć. Niestymulowane próbki śliny pobiera się od osobnika w celu pomiaru i rejestracji pH śliny po 15, 30 i 45 minutach po zakończeniu płukania gardła przez osobnika jako interwencji.
Eksperymentalny: Group 3: 0.2% chlorhexidine

The subject collects the unstimulated saliva in a sterile glass dish for the measurement of baseline pH of the saliva. The subject is then given 100 ml of test mixed fruit juice, Tropicana® Mixed Fruit Juice, (PepsiCo, Inc) to drink. The subject will sip, swish and swallow the drink within 2 minutes.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva after 5 and 15 minutes of consumption of the test mixed fruit juice.

The subject will use 10 ml of 0.2% Chlorhexidine mouth rinse (Rexidine®, Indoco Remidies Ltd, Mumbai, India) to swish for 60 seconds and spit. Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva at 15, 30 and 45 minutes after the subject completes the gargle as an intervention.

The subject will use 10 ml of 0.2% Chlorhexidine mouth rinse (Rexidine®, Indoco Remidies Ltd, Mumbai, India) to swish for 60 seconds and spit. Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva at 15, 30 and 45 minutes after the subject completes the gargle as an intervention.
Inne nazwy:
  • Reksydyna®
Eksperymentalny: Group 4: fluoridated tooth paste

The subject collects the unstimulated saliva in a sterile glass dish for the measurement of baseline pH of the saliva. The subject is then given 100 ml of test mixed fruit juice, Tropicana® Mixed Fruit Juice, (PepsiCo, Inc) to drink. The subject will sip, swish and swallow the drink within 2 minutes.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva after 5 and 15 minutes of consumption of the test mixed fruit juice.

The subject will Brush with fluoridated toothpaste (Colgate Total®, Colgate-Palmolive Company, Mumbai, India) for 2 minutes using soft brush.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva at 15, 30 and 45 minutes after the subject completes the brushing as an intervention.

Pacjent będzie szczotkował zęby pastą z fluorem (Colgate Total®, Colgate-Palmolive Company, Mumbai, Indie) przez 2 minuty za pomocą miękkiej szczoteczki.

Niestymulowane próbki śliny pobiera się od osobnika w celu pomiaru i odnotowania pH śliny po 15, 30 i 45 minutach od zakończenia stosowania pasty do zębów przez osobnika jako interwencji.

Inne nazwy:
  • Colgate Total®
Eksperymentalny: Group 5: Polyol containing gum

The subject collects the unstimulated saliva in a sterile glass dish for the measurement of baseline pH of the saliva. The subject is then given 100 ml of test mixed fruit juice, Tropicana® Mixed Fruit Juice, (PepsiCo, Inc) to drink. The subject will sip, swish and swallow the drink within 2 minutes.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva after 5 and 15 minutes of consumption of the test mixed fruit juice.

The subject will chew polyol containing gum (Orbit®, Wrigley Company) for 5 minutes and spit.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva at 15, 30 and 45 minutes after the subject completes the chewing gum as an intervention.

The subject will chew polyol containing gum (Orbit®, WrigleyCompany) for 5 minutes and spit.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva at 15, 30 and 45 minutes after the subject completes chewing as an intervention.

Inne nazwy:
  • Orbita®
Eksperymentalny: Group 6: 1% sodium bicarbonate solution

The subject collects the unstimulated saliva in a sterile glass dish for the measurement of baseline pH of the saliva. The subject is then given 100 ml of test mixed fruit juice, Tropicana® Mixed Fruit Juice, (PepsiCo, Inc) to drink. The subject will sip, swish and swallow the drink within 2 minutes.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva after 5 and 15 minutes of consumption of the test mixed fruit juice.

The subject will use 10 ml freshly prepared 1% sodium bicarbonate w/v solution to swish for 60 seconds and spit.

Unstimulated saliva samples are collected from the subject to measure and record the pH of saliva at 15, 30 and 45 minutes after the subject completes the gargle as an intervention.

Pacjent użyje 10 ml świeżo przygotowanego 1% roztworu wodorowęglanu sodu w/v do swędzenia przez 60 sekund i splunięcia.

Niestymulowane próbki śliny pobiera się od osobnika w celu pomiaru i rejestracji pH śliny po 15, 30 i 45 minutach po zakończeniu płukania gardła przez osobnika jako interwencji.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
pH of saliva at baseline
Ramy czasowe: 0 minute
All subjects in all groups collects the unstimulated saliva in a sterile glass dish for the measurement of baseline pH of the saliva. The subject will give the saliva sample just before being exposed to the test mixed fruit juice by swishing 100ml of Tropicana® Mixed Fruit Juice in mouth for 2 minutes and then drinking it The outcome accessor is blinded to origin of sample (from which group).
0 minute

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
pH of Saliva 5 minutes after exposure to test mixed fruit juice
Ramy czasowe: 5 minutes
All subjects will be given 100 ml of test mixed fruit juice, Tropicana® Mixed Fruit Juice to drink. The subject will sip, swish and swallow the drink within 2 minutes. Five minutes after this, each subject will give unstimulated saliva in a sterile dish for measurement of saliva - 5minutes after exposure to test mixed fruit juice. The outcome accessor is blinded to the origin of sample (from which group).
5 minutes
pH of Saliva 15 minutes after exposure to test mixed fruit juice
Ramy czasowe: 15 minutes
All subjects will give unstimulated saliva in a sterile dish for measurement of saliva -15minutes after exposure to test mixed fruit juice. The outcome accessor is blinded to the origin of sample (from which group).
15 minutes
pH of Saliva 30 minutes after exposure to test mixed fruit juice
Ramy czasowe: 30 minutes
All subjects from all six (5 test and 1 comparator) groups will perform the assigned intervention as per schedule at time 15minutes post exposure to mixed fruit juice and shall give unstimulated saliva in a sterile dish for measurement of saliva -30minutes after exposure to test mixed fruit juice or in other words 15minutes after assigned intervention. The outcome accessor is blinded to the origin of sample (from which group).
30 minutes
pH of Saliva 45 minutes after exposure to test mixed fruit juice
Ramy czasowe: 45 minutes
All subjects from all six (5 test and 1 comparator) groups will perform the assigned intervention as per given schedule at time 15minutes post exposure to mixed fruit juice and shall give unstimulated saliva in a sterile dish for measurement of saliva -45minutes after exposure to test mixed fruit juice or in other words 30minutes after assigned intervention. The outcome accessor is blinded to the origin of sample (from which group).
45 minutes
pH of Saliva 60 minutes after exposure to test mixed fruit juice
Ramy czasowe: 60 minutes
All subjects from all six (5 test and 1 comparator) groups will perform the assigned intervention as per given schedule at time 15 minutes post exposure to mixed fruit juice and shall give unstimulated saliva in a sterile dish for measurement of saliva -60minutes after exposure to test mixed fruit juice or in other words 45minutes after assigned intervention. The outcome accessor is blinded to the origin of sample (from which group).
60 minutes

Współpracownicy i badacze

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Sponsor

Publikacje i pomocne linki

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Publikacje ogólne

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

25 kwietnia 2018

Zakończenie podstawowe (Rzeczywisty)

5 lipca 2018

Ukończenie studiów (Rzeczywisty)

5 grudnia 2018

Daty rejestracji na studia

Pierwszy przesłany

17 kwietnia 2018

Pierwszy przesłany, który spełnia kryteria kontroli jakości

17 kwietnia 2018

Pierwszy wysłany (Rzeczywisty)

27 kwietnia 2018

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

6 grudnia 2018

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

5 grudnia 2018

Ostatnia weryfikacja

1 grudnia 2018

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • UDMRI_Sal_pH_F
  • U1111-1212-3732 (Identyfikator rejestru: WHO International Clinical Trials Registry Platform (ICTRP))

Plan dla danych uczestnika indywidualnego (IPD)

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NIEZDECYDOWANY

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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